Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity-Reference-Cited by-同舟云学术

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Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity

Published:2002-10-01 Issue:4-5 Volume:111 Page:428-434
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Génin Emmanuelle,Huebner Angela,Jaillard Christine,Faure Armelle,Halaby Georges,Saka Nurçin,Clark Adrian,Durand Philippe,Bégeot Martine,Naville Danielle

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0806-3.pdf

Cited by 26 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

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2. Anterior Pituitary and Pars Intermedia Space;Hormonal Signaling in Biology and Medicine;2020

3. ACTH Receptor (MC2R) Specificity: What Do We Know About Underlying Molecular Mechanisms?;Frontiers in Endocrinology;2017-02-06

4. 8q13.1-q13.2 Deletion Associated With Inferior Cerebellar Vermian Hypoplasia and Digital Anomalies: A New Syndrome?;Pediatric Neurology;2015-02

5. Molecular Genetics of Inherited Glucocorticoid Deficiency;eLS;2014-10-15

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