Exome Sequencing is a Valuable Approach in Critically Ill Patients with Suspected Monogenic Disease: Diagnosis of X-linked Centronuclear Myopathy in Preterm Twins

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Exome Sequencing is a Valuable Approach in Critically Ill Patients with Suspected Monogenic Disease: Diagnosis of X-linked Centronuclear Myopathy in Preterm Twins. / Johannsen, Jessika; Hempel, Maja; Diehl, Thilo; Haack, Tobias B; Denecke, Jonas.

In: PEDIATR NEONATOL, Vol. 58, No. 5, 10.2017, p. 458-459.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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@article{feaf04593b044fccafb445f5ffb57d09,
title = "Exome Sequencing is a Valuable Approach in Critically Ill Patients with Suspected Monogenic Disease: Diagnosis of X-linked Centronuclear Myopathy in Preterm Twins",
author = "Jessika Johannsen and Maja Hempel and Thilo Diehl and Haack, {Tobias B} and Jonas Denecke",
year = "2017",
month = oct,
doi = "10.1016/j.pedneo.2016.05.007",
language = "English",
volume = "58",
pages = "458--459",
journal = "PEDIATR NEONATOL",
issn = "1875-9572",
publisher = "Elsevier (Singapore) Pte Ltd",
number = "5",

}

RIS

TY - JOUR

T1 - Exome Sequencing is a Valuable Approach in Critically Ill Patients with Suspected Monogenic Disease: Diagnosis of X-linked Centronuclear Myopathy in Preterm Twins

AU - Johannsen, Jessika

AU - Hempel, Maja

AU - Diehl, Thilo

AU - Haack, Tobias B

AU - Denecke, Jonas

PY - 2017/10

Y1 - 2017/10

U2 - 10.1016/j.pedneo.2016.05.007

DO - 10.1016/j.pedneo.2016.05.007

M3 - SCORING: Journal article

C2 - 27989427

VL - 58

SP - 458

EP - 459

JO - PEDIATR NEONATOL

JF - PEDIATR NEONATOL

SN - 1875-9572

IS - 5

ER -