Prof. Dr. ID: 40416
Kerstin Kutsche
Publications
- 2003
Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling
Rosenberger, G., Jantke, I., Gal, A. & Kutsche, K., 15.01.2003, In: HUM MOL GENET. 12, 2, p. 155-67 13 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Zimmermann-Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions
Stefanova, M., Atanassov, D., Krastev, T., Fuchs, S. & Kutsche, K., 15.03.2003, In: AM J MED GENET A. 117A, 3, p. 289-94 6 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2006
AlphaPIX and betaPIX and their role in focal adhesion formation
Rosenberger, G. & Kutsche, K., 2006, In: EUR J CELL BIOL. 85, 3-4, p. 265-274 10 p., 3-4.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
Rau, I., Morleo, M., Rosenberger, G., Iaconis, D., Orth, U., Meinecke, P., Lerer, I., Ballabio, A., Gal, A., Franco, B. & Kutsche, K., 2006, In: AM J HUM GENET. 79, 5, p. 878-889 5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody.
Martinez-Garay, I., Rustom, A., Gerdes, H-H. & Kutsche, K., 2006, In: GENOMICS. 87, 2, p. 243-253 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2007
A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
Martínez-Garay, I., Tomás, M., Oltra, S., Ramser, J., Moltó, M. D., Prieto, F., Meindl, A., Kutsche, K. & Martínez, F., 2007, In: EUR J HUM GENET. 15, 1, p. 29-34 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Candidate loci for Zimmermann-Laband syndrome at 3p14.3.
Hyung-Goo, K., Higgins Anne, W., Herrick Steven, R., Kishikawa, S., Nicholson, L., Kutsche, K., Ligon Azra, H., Harris David, J., Macdonald Marcy, E., Bruns Gail, A. P., Morton Cynthia, C., Quade Bradley, J. & Gusella James, F., 2007, In: AM J MED GENET A. 143, 2, p. 107-111 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.
Zenker, M., Lehmann, K., Schulz, A. L., Barth, H., Hansmann, D., Koenig, R., Korinthenberg, R., Kreiss-Nachtsheim, M., Meinecke, P., Morlot, S., Mundlos, S., Quante, A. S., Raskin, S., Schnabel, D., Wehner, L-E., Kratz, C. P., Horn, D. & Kutsche, K., 2007, In: J MED GENET. 44, 2, p. 131-135 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
Abo-Dalo, B., Kim, H-G., Roes, M., Stefanova, M., Higgins, A., Shen, Y., Mundlos, S., Quade, B. J., Gusella, J. F. & Kutsche, K., 2007, In: AM J MED GENET A. 143, 22, p. 2668-2674 22.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?
Rau, I., Shaw, G. M. & Kutsche, K., 2007, In: MOL VIS. 13, p. 1475-1482Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
Rau, I., Rauch, A., Orth, U., Schwarzer, U., Trautmann, U. & Kutsche, K., 2007, In: EUR J MED GENET. 50, 6, p. 421-431 6.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome.
Zenker, M., Horn, D., Wieczorek, D., Allanson, J., Pauli, S., van der Burgt, I., Doerr, H-G., Gaspar, H., Hofbeck, M., Gillessen-Kaesbach, G., Koch, A., Meinecke, P., Mundlos, S., Nowka, A., Rauch, A., Reif, S., von Schnakenburg, C., Seidel, H., Wehner, L-E., Zweier, C., Bauhuber, S., Matejas, V., Kratz, C. P., Thomas, C. & Kutsche, K., 2007, In: J MED GENET. 44, 10, p. 651-656 10.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2008
AlphaPIX Rho GTPase guanine nucleotide exchange factor regulates lymphocyte functions and antigen receptor signaling.
Missy, K., Hu, B., Schilling, K., Harenberg, A., Sakk, V., Kuchenbecker, K., Kutsche, K. & Fischer, K-D., 2008, In: MOL CELL BIOL. 28, 11, p. 3776-3789 11.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Disruption of neurexin 1 associated with autism spectrum disorder.
Kim, H-G., Kishikawa, S., Higgins, A. W., Seong, I-S., Donovan Diana, J., Shen, Y., Lally, E., Weiss, L. A., Najm, J., Kutsche, K., Descartes, M., Holt, L., Braddock, S., Troxell, R., Kaplan, L., Volkmar, F., Klin, A., Tsatsanis, K., Harris, D. J., Noens, I., Pauls, D. L., Daly, M. J., MacDonald, M. E., Morton, C. C., Quade Bradley, J. & Gusella, J. F., 2008, In: AM J HUM GENET. 82, 1, p. 199-207 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
Schulz, A. L., Albrecht, B., Arici, C., van der Burgt, I., Buske, A., Gillessen-Kaesbach, G., Heller, R., Horn, D., Hübner, C., Korenke, G. C., König, R., Kress, W., Krüger, G., Meinecke, P., Mücke, J., Plecko, B., Rossier, E., Schinzel, A., Schulze, A., Seemanova, E., Seidel, H., Spranger, S., Tuysuz, B., Uhrig, S., Wieczorek, D., Kutsche, K. & Zenker, M., 2008, In: CLIN GENET. 73, 1, p. 62-70 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum.
Najm, J., Horn, D., Rau, I., Golden, J. A., Chizhikov, V. V., Jyotsna, S., Christian, S. L., Ullmann, R., Kuechler, A., Haas, C. A., Flubacher, A., Charnas, L. R., Uyanik, G., Frank, U., Klopocki, E., Dobyns, W. B. & Kutsche, K., 2008, In: NAT GENET.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
Abo-Dalo, B., Roes, M., Canún, S., Delatycki, M., Gillessen-Kaesbach, G., Hrytsiuk, I., Jung, C., Kerr, B., Mowat, D., Seemanova, E., Steiner, C. E., Stewart, H., Thierry, P., van Buggenhout, G., White, S., Zenker, M. & Kutsche, K., 2008, In: CLIN DYSMORPHOL. 17, 3, p. 181-185 3.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.
Morris-Rosendahl, D. J., Najm, J., Lachmeijer, A. M. A., Sztriha, L., Martins, M., Kuechler, A., Haug, V., Zeschnigk, C., Martin, P., Santos, M., Vasconcelos, C., Omran, H., Kraus, U., Van der Knaap, M. S., Schuierer, G., Kutsche, K. & Uyanik, G., 2008, In: CLIN GENET. 74, 5, p. 425-433 5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2009
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.
Gremer, L., Alessandro, D. L., Merbitz-Zahradnik, T., Dallapiccola, B., Morlot, S., Tartaglia, M., Kutsche, K., Ahmadian, M. R. & Rosenberger, G., 2009, In: HUM MOL GENET.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
Harmsen, M-B., Azzarello-Burri, S., González, G., Mar, M., Gillessen-Kaesbach, G., Meinecke, P., Müller, D., Rauch, A., Rossier, E., Seemanova, E., Spaich, C., Steiner, B., Wieczorek, D., Kutsche, K. & Kutsche, K., 2009, In: EUR J HUM GENET. 17, 10, p. 1207-1215 10.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.
Cordeddu, V., Elia, D. S., Pennacchio, L. A., Ma'ayan, A., Sarkozy, A., Fodale, V., Cecchetti, S., Cardinale, A., Martin, J., Schackwitz, W., Lipzen, A., Zampino, G., Mazzanti, L., Digilio, M. C., Martinelli, S., Flex, E., Lepri, F., Deborah, B., Kutsche, K., Ferrero, G. B., Anichini, C., Selicorni, A., Rossi, C., Tenconi, R., Zenker, M., Merlo, D., Dallapiccola, B., Iyengar, R., Bazzicalupo, P., Gelb, B. D. & Tartaglia, M., 2009, In: NAT GENET. 41, 9, p. 1022-1026 9.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Oncogenic HRAS mutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome.
Rosenberger, G., Meien, S. & Kutsche, K., 2009, In: HUM MUTAT. 30, 3, p. 352-362 3.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2010
A restricted spectrum of NRAS mutations causes Noonan syndrome.
Cirstea, I. C., Kutsche, K., Dvorsky, R., Gremer, L., Carta, C., Horn, D., Roberts, A. E., Lepri, F., Merbitz-Zahradnik, T., König, R., Kratz, C. P., Pantaleoni, F., Dentici, M. L., Joshi, V. A., Kucherlapati, R. S., Mazzanti, L., Mundlos, S., Patton, M. A., Silengo, M. C., Rossi, C., Zampino, G., Digilio, C., Stuppia, L., Seemanova, E., Pennacchio, L. A., Gelb, B. D., Dallapiccola, B., Wittinghofer, A., Ahmadian, M. R., Tartaglia, M. & Zenker, M., 2010, In: NAT GENET. 42, 1, p. 27-29 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
A severe form of the X-linked microphthalmia with linear skin defects syndrome in a female newborn.
Steichen-Gersdorf, E., Griesmaier, E., Pientka, F. K., Kotzot, D. & Kutsche, K., 2010, In: CLIN DYSMORPHOL. 19, 2, p. 82-84 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Large intragenic deletions of the NF2 gene: breakpoints and associated phenotypes.
Abo-Dalo, B., Kutsche, K., Mautner, V. F. & Kluwe, L., 2010, In: GENE CHROMOSOME CANC. 49, 2, p. 171-175 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
Endele, S., Rosenberger, G., Geider, K., Popp, B., Tamer, C., Stefanova, I., Milh, M., Kortüm, F., Fritsch, A., Pientka, F. K., Hellenbroich, Y., Kalscheuer, V. M., Kohlhase, J., Moog, U., Rappold, G., Rauch, A., Ropers, H-H., von Spiczak, S., Tönnies, H., Villeneuve, N., Villard, L., Zabel, B., Zenker, M., Laube, B., Reis, A., Wieczorek, D., Lionel, V. M. & Kutsche, K., 2010, In: NAT GENET. 42, 11, p. 1021-1026 11.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Neuro-kardio-fazio-kutane Syndrome: Überlappende Phänotypen mit gemeinsamem molekularem Signalweg interdisziplinäres Betreuungskonzept
Mautner, V. F., Nguyen, R., Bernhardt, A., Von Kodolitsch, Y., Zenker, M. & Kutsche, K., 2010, In: MED GENET-BERLIN. 1, p. 10-19Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
The face of Noonan syndrome: Does phenotype predict genotype.
Allanson, J. E., Bohring, A., Dörr, H-G., Dufke, A., Gillessen-Kaesbach, G., Horn, D., König, R., Kratz, C. P., Kutsche, K., Pauli, S., Raskin, S., Rauch, A., Turner, A., Wieczorek, D. & Zenker, M., 2010, In: AM J MED GENET A. 152, 8, p. 1960-1966 8.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I.
Fabretto, A., Kutsche, K., Harmsen, M-B., Demarini, S., Gasparini, P., Fertz, M. C. & Zenker, M., 2010, In: EUR J MED GENET. 53, 5, p. 322-324 5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation
Girisha, K. M., Lewis, L. E., Phadke, S. R. & Kutsche, K., 01.11.2010, In: AM J MED GENET A. 152A, 11, p. 2861-4 4 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2011
Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.
Kortüm, F., Chyrek, M., Fuchs, S., Albrecht, B., Gillessen-Kaesbach, G., Mütze, U., Seemanova, E., Tinschert, S., Wieczorek, D., Rosenberger, G. & Kutsche, K., 2011, In: MOL SYNDROMOL. 2, 1, p. 27-34 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Phenotypic spectrum associated with CASK loss-of-function mutations.
Moog, U., Kutsche, K., Kortüm, F., Chilian, B., Bierhals, T., Apeshiotis, N., Balg, S., Chassaing, N., Coubes, C., Das, S., Engels, H., Hilde, V. E., Grasshoff, U., Heise, M., Isidor, B., Jarvis, J., Koehler, U., Martin, T., Oehl-Jaschkowitz, B., Ortibus, E., Pilz, D. T., Prabhakar, P., Rappold, G., Rau, I., Rettenberger, G., Schlüter, G., Scott, R. H., Shoukier, M., Wohlleber, E., Zirn, B., Dobyns, W. B. & Uyanik, G., 2011, In: J MED GENET. 48, 11, p. 741-751 11.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
Kortüm, F., Das, S., Flindt, M., Morris-Rosendahl, D. J., Stefanova, I., Goldstein, A., Horn, D., Klopocki, E., Kluger, G., Martin, P., Rauch, A., Roumer, A., Saitta, S., Walsh, L. E., Wieczorek, D., Uyanik, G., Kutsche, K. & Dobyns, W. B., 2011, In: J MED GENET. 48, 6, p. 396-406 6.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2012
Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.
Dalal, A., Bhavani, G., Lakshmi, S., Bierhals, T., Bierhals, T., Nandineni, M. R., Danda, S., Danda, D., Shah, H., Vijayan, S., Gowrishankar, K., Phadke, S. R., Bidchol, A. M., Rao, A. P., Kutsche, K., Kutsche, K. & Girisha, K. M., 2012, In: AM J MED GENET A. 158A, 11, p. 2820-2828 11.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits.
Ramakers, G. J. A., Wolfer, D., Rosenberger, G., Kuchenbecker, K., Kreienkamp, H-J., Prange-Kiel, J., Rune, G. M., Richter, K., Langnaese, K., Masneuf, S., Bösl, M. R., Fischer, K-D., Krugers, H. J., Lipp, H-P., van Galen, E. & Kutsche, K., 2012, In: HUM MOL GENET. 21, 2, p. 268-286 2.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease.
Indrieri, A., van Rahden, V., Alexandra, V., Tiranti, V., Morleo, M., Iaconis, D., Tammaro, R., D'Amato, I., Conte, I., Maystadt, I., Demuth, S., Kutsche, K., Kutsche, K., Zeviani, M. & Franco, B., 2012, In: AM J HUM GENET. 91, 5, p. 942-949 5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
The 5-phosphatase OCRL mediates retrograde transport of the mannose 6-phosphate receptor by regulating a Rac1-cofilin signalling module.
van Rahden, V., Brand, K., Najm, J., Heeren, J., Heeren, J., Braulke, T., Kutsche, K. & Kutsche, K., 2012, In: HUM MOL GENET. 21, 23, p. 5019-5038 23.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.
Kim, H-G., Kim, H-T., Leach, N. T., Lan, F., Ullmann, R., Silahtaroglu, A., Kurth, I., Nowka, A., Seong, I. S., Shen, Y., Talkowski, M. E., Ruderfer, D., Lee, J-H., Glotzbach, C., Ha, K., Kjaergaard, S., Levin, A. V., Romeike, B. F., Kleefstra, T., Bartsch, O., Elsea, S. H., Jabs, E. W., MacDonald, M. E., Harris, D. J., Quade, B. J., Ropers, H-H., Shaffer, L. G., Kutsche, K., Layman, L. C., Tommerup, N., Kalscheuer, V. M., Shi, Y., Morton, C. C., Kim, C-H. & Gusella, J. F., 2012, In: AM J HUM GENET. 91, 1, p. 56-72 1.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Two cases with severe lethal course of Costello syndrome associated with HRAS p.G12C and p.G12D.
Lorenz, S., Petersen, C., Kordaß, U., Seidel, H., Zenker, M. & Kutsche, K., 2012, In: EUR J MED GENET. 55, 11, p. 615-619 11.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features.
Lozić, B., Ljubković, J., Pandurić, D. G., Saltvig, I., Kutsche, K., Krželj, V. & Zemunik, T., 01.12.2012, In: BRAZ J MED BIOL RES. 45, 12, p. 1315-1319 5 p., 12.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2013
Estrogen and the male hippocampus: genetic variation in the aromatase gene predicting serum estrogen is associated with hippocampal gray matter volume in men
Bayer, J., Rune, G., Kutsche, K., Schwarze, U., Kalisch, R., Büchel, C. & Sommer-Blöchl, T., 01.02.2013, In: HIPPOCAMPUS. 23, 2, p. 117-21 5 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Expanding the phenotype associated with 17q12 duplication: case report and review of the literature
Bierhals, T., Maddukuri, S. B., Kutsche, K. & Girisha, K. M., 01.02.2013, In: AM J MED GENET A. 161A, 2, p. 352-9 8 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Exon 2 duplication of the MID1 gene in a patient with a mild phenotype of Opitz G/BBB syndrome
Hüning, I., Kutsche, K., Rajaei, S., Erlandsson, A., Lovmar, L., Rundberg, J. & Stefanova, M., 01.04.2013, In: EUR J MED GENET. 56, 4, p. 188-91 4 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Pontocerebellar hypoplasia type 2 and TSEN2: review of the literature and two novel mutations
Bierhals, T., Korenke, G. C., Uyanik, G. & Kutsche, K., 01.06.2013, In: EUR J MED GENET. 56, 6, p. 325-30 6 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm
Leutermann, R., Sheikhzadeh, S., Brockstädt, L., Rybczynski, M., van Rahden, V., Kutsche, K., Kodolitsch, Y. & Rosenberger, G., 06.11.2013, In: EUR J HUM GENET. 22, p. 944-948Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
CASK-Related Disorders
Moog, U., Uyanik, G. & Kutsche, K., 26.11.2013, In: GeneReviews®.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci
Chilian, B., Abdollahpour, H., Bierhals, T., Haltrich, I., Fekete, G., Nagel, I., Rosenberger, G. & Kutsche, K., 01.12.2013, In: CLIN GENET. 84, 6, p. 560-5 6 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition
Brownstein, C. A., Towne, M. C., Luquette, L. J., Harris, D. J., Marinakis, N. S., Meinecke, P., Kutsche, K., Campeau, P. M., Yu, T. W., Margulies, D. M., Agrawal, P. B. & Beggs, A. H., 01.12.2013, In: EUR J MED GENET. 56, 12, p. 678-82 5 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2014
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation
Sheikhzadeh, S., Sondermann, C., Rybczynski, M., Habermann, C. R., Brockstädt, L., Keyser, B., Kaemmerer, H., Mir, T., Staebler, A., Robinson, P. N., Kutsche, K., Berger, J., Blankenberg, S. & Kodolitsch, Y., 2014, In: CLIN GENET. 86, 3, p. 238-245Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Dermatoscopic aspects of the microphthalmia with linear skin defects (MLS) syndrome
de Almeida, H. L., Rossi, G., de Abreu, L. B., Bergamaschi, C., da Silva, A. B. & Kutsche, K., 2014, In: AN BRAS DERMATOL. 89, 1, p. 180-1 2 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review