Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism-Reference-Cited by-同舟云学术

Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism

Published:2003-05 Issue:5 Volume:53 Page:749-755
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

De Sanctis Luisa,Romagnolo Damiano,Olivero Martina,Buzi Fabio,Maghnie Mohamad,Scirè Giuseppe,Crinò Antonino,Baroncelli Giampiero Igli,Salerno Mariacarolina,Di Maio Salvatore,Cappa Marco,Grosso Salvatore,Rigon Franco,Lala Roberto,De Sanctis Carlo,Dianzani Irma

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference42 articles.

1. Pseudohypoparathyroidism

2. Pseudohypoparathyroidism: defective excretion of 3′,5′-AMP in response to parathyroid hormone

3. Heterotrimeric G proteins

Cited by 52 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. Albright Hereditary Osteodystrophy;Genetic Syndromes;2023

2. Evaluating the variety of GNAS inactivation disorders and their clinical manifestations in 11 Chinese children;BMC Endocrine Disorders;2022-03-16

3. Dermale Osteome als erstes Symptom einer hereditären Albright‐Osteodystrophie bei einem zehn Monate alten Mädchen;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-07

4. Dermal osteomata as first symptom of Albright’s hereditary osteodystrophy in a 10‐month‐old girl;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-03-25

5. Hypocalcemic disorders;Best Practice & Research Clinical Endocrinology & Metabolism;2018-10