Borjeson-Forssman-Lehmann Syndrome and Multiple Pituitary Hormone Deficiency-Reference-Cited by-同舟云学术

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Borjeson-Forssman-Lehmann Syndrome and Multiple Pituitary Hormone Deficiency

Published:2003-01 Issue:9 Volume:16 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Birrcll G.,Lampe A.,Richmond S.,Bruce S.N.,Gecz J.,Lower K.,Wright M.,Chectham T.D.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2003.16.9.1295/pdf

Reference10 articles.

1. A new step understood in the cascade of tissue-specific regulators orchestrating pituitary lineage determination: the Prophet of Pit-1 (Prop-1)

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

3. Heritable Disorders of Pituitary Development

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Downregulation of the GHRH/GH/IGF-1 axis in a mouse model of Börjeson-Forssman-Lehman Syndrome;Development;2020-01-01

2. Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity;Gene Expression Patterns;2007-10

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