An association with hypopituitarism and 9q subtelomere deletion syndrome-Reference-Cited by-同舟云学术

An association with hypopituitarism and 9q subtelomere deletion syndrome

Published:2018-10-25 Issue:12 Volume:6 Page:2371-2375
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Higuchi Shinji¹,Takagi Masaki²³^ORCID,Takeda Ryojun⁴^ORCID,Yoshihashi Hiroshi⁴,Narumi Satoshi²⁵,Hasegawa Tomonobu²

Affiliation:

1. Department of Pediatric Endocrinology and MetabolismChildren’s Medical CenterOsaka City General Hospital Osaka Japan

2. Department of PediatricsKeio University School of Medicine Tokyo Japan

3. Kojiya Child Clinic Tokyo Japan

4. Department of Medical GeneticsTokyo Metropolitan Children’s Medical Center Tokyo Japan

5. Department of Molecular EndocrinologyNational Research Institute for Child Health and Development Tokyo Japan

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.1591

Reference11 articles.

1. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype

2. Expanding the phenotypic profile of Kleefstra syndrome: A female with low-average intelligence and childhood apraxia of speech

3. The chromosome 9q subtelomere deletion syndrome

4. Update on Kleefstra syndrome;Willemsen MH;Mol Syndromol,2012

5. Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone‐releasing hormone (LHRH) neurons;Kramer PR;Genes Dev,2000

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