Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia-Reference-Cited by-同舟云学术

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Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

Published:1992-10-08 Issue:15 Volume:327 Page:1069-1074
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Bilous Rudolf W.,Murty George,Parkinson David B.,Thakker Rajesh V.,Coulthard Malcolm G.,Burn John,Mathias David,Kendall-Taylor Pat

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJM199210083271506

Cited by 158 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. HDR syndrome: Large cohort and systematic review;Clinical Genetics;2024-06-28

2. Hypoparathyroidism, deafness and renal dysplasia syndrome with bilateral cataract and bicornuate uterus caused by a de novo GATA3 mutation;Exploration of Endocrine and Metabolic Diseases;2024-05-27

3. HDR syndrome, detected in the neonatal period by newborn hearing screening;Auris Nasus Larynx;2024-04

4. A novel GATA3 frameshift mutation causes hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome;Molecular Genetics and Metabolism Reports;2024-03

5. Shared features in ear and kidney development – implications for oto-renal syndromes;Disease Models & Mechanisms;2024-02-01

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