Transient Congenital Hypoparathyroidism and 22q11 Deletion-Reference-Cited by-同舟云学术

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Transient Congenital Hypoparathyroidism and 22q11 Deletion

Published:2000-01 Issue:6 Volume:13 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

García-García E.,Camacho-Alonso J.,Gómez-Rodríguez M.J.,del Castillo Ε.,Martinez-Aedo M.J.,López-Siguero J.P.

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.2000.13.6.659/pdf

Reference16 articles.

1. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

2. Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion

Cited by 6 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. Perinatal Calcium and Phosphorus Metabolism;Nephrology and Fluid/electrolyte Physiology;2019

2. Perinatal Calcium and Phosphorus Metabolism;Nephrology and Fluid/Electrolyte Physiology: Neonatology Questions and Controversies;2012

3. Head and neck manifestations of 22q11.2 deletion syndromes;European Archives of Oto-Rhino-Laryngology;2011-08-23

4. Endocrine Manifestations of Chromosome 22q11.2 Microdeletion Syndrome;Hormone Research in Paediatrics;2005

5. Hipoparatiroidismo en un adulto como única manifestación de microdeleción del cromosoma 22q11;Medicina Clínica;2002-01

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