Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
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Chromatin Remodeling BAF (SWI/SNF) Complexes in Neural Development and Disorders.Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.Diagnostic use of computational retrotransposon detection: Successful definition of pathogenetic mechanism in a ciliopathy phenotype.
P2860
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
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Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@en
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@nl
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label
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@en
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@nl
prefLabel
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@en
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation.
@nl
P2093
P2860
P356
P1476
Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation
@en
P2093
Hiroshi Yoshihashi
Kenjiro Kosaki
Masataka Honda
Sahoko Miyama
Takao Takahashi
Toshiki Takenouchi
Yuri Sakaguchi
P2860
P304
P356
10.1002/AJMG.A.37861
P407
P577
2016-08-11T00:00:00Z