New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect
about
Fetal magnetic resonance imaging (MRI): a tool for a better understanding of normal and abnormal brain development.Transcription factor ISL1 is essential for pacemaker development and function.Identification and analysis of a novel dimerization domain shared by various members of c-Jun N-terminal kinase (JNK) scaffold proteins.
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New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect
description
article
@en
im Dezember 2011 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2011
@uk
name
New recessive syndrome of micr ...... enital heart conduction defect
@en
New recessive syndrome of micr ...... enital heart conduction defect
@nl
type
label
New recessive syndrome of micr ...... enital heart conduction defect
@en
New recessive syndrome of micr ...... enital heart conduction defect
@nl
prefLabel
New recessive syndrome of micr ...... enital heart conduction defect
@en
New recessive syndrome of micr ...... enital heart conduction defect
@nl
P2093
P2860
P50
P356
P1476
New recessive syndrome of micr ...... enital heart conduction defect
@en
P2093
Ghada M H Abdel Salam
Sahar N Saleem
Shifteh Sattar
P2860
P304
P356
10.1002/AJMG.A.34078
P407
P577
2011-12-01T00:00:00Z