Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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im August 2002 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2002

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name

Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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Bases Genéticas dos Distúrbios de Crescimento

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P1476

Bases Genéticas dos Distúrbios de Crescimento

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P2093

Alexander A. de Lima Jorge

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Berenice B. de Mendonça

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Ivo J. Prado Arnhold

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Luciani R. S. de Carvalho

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Silvia Leão Corral Souza

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Suemi Marui

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P2860

Differential activation of pituitary hormone genes by human Lhx3 isoforms with distinct DNA binding properties

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Mutations of the growth hormone receptor in children with idiopathic short stature. The Growth Hormone Insensitivity Study Group

Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse

Pituitary dwarfism in the R271W Pit-1 gene mutation

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

PHOG, a candidate gene for involvement in the short stature of Turner syndrome

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

P304

444-456

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P31

scholarly article

P356

10.1590/S0004-27302002000400016

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P433

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P478

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P577

2002-08-01T00:00:00Z

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