Complex Genomic Rearrangement Within the<i>GNAS</i>Region Associated With Familial Pseudohypoparathyroidism Type 1b-Reference-Cited by-同舟云学术

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Complex Genomic Rearrangement Within theGNASRegion Associated With Familial Pseudohypoparathyroidism Type 1b

Published:2016-07 Issue:7 Volume:101 Page:2623-2627
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Nakamura Akie,Hamaguchi Erika,Horikawa Reiko,Nishimura Yasuyuki,Matsubara Keiko,Sano Shinichiro,Nagasaki Keisuke,Matsubara Yoichi,Umezawa Akihiro,Tajima Toshihiro,Ogata Tsutomu,Kagami Masayo,Okamura Kohji,Fukami Maki

Publisher

The Endocrine Society

Cited by 25 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. Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B;JCI Insight;2024-12-20

2. (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B;European Journal of Endocrinology;2023-12-01

3. Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia;The Journal of Clinical Endocrinology & Metabolism;2023-10-25

4. Single-exon deletions ofZNRF3exon 2 cause congenital adrenal hypoplasia;2023-06-16

5. A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B;Bone;2022-04

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