Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndrome.
about
Simpson-Golabi-Behmel syndrome types I and II.Single gene disorders associated with congenital diaphragmatic hernia.Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature.A patient with Simpson-Golabi-Behmel syndrome, biliary cirrhosis and successful liver transplantation.Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome.
P2860
Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndrome.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
@wuu
2005年学术文章
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2005年学术文章
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2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
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2005年學術文章
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2005年學術文章
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name
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@en
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@nl
type
label
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@en
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@nl
prefLabel
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@en
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@nl
P2093
P356
P1476
Clinical and molecular studies ...... impson-Golabi-Behmel syndrome.
@en
P2093
Antonio González-Meneses
Germán Rodríguez-Criado
Giovanni Neri
Ignacio Gómez de Terreros
Luis Magano
Mabel Segovia
Pablo Lapunzina
Ricardo Gracia
Rita Valdéz
P304
P356
10.1002/AJMG.A.30920
P407
P577
2005-10-01T00:00:00Z