Abnormal bone mineral content and density in people with tetrasomy 18p-Reference-Cited by-同舟云学术

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Abnormal bone mineral content and density in people with tetrasomy 18p

Published:2019-01-13 Issue:3 Volume:179 Page:417-422
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Moreira Alvaro¹²,Das Hrishikesh¹^ORCID,Hasi‐Zogaj Minire³,Soileau Bridgette³,Hill Annice³,Bruder Jan M.⁴,Hale Daniel E.²⁵,Cody Jannine D.²³^ORCID

Affiliation:

1. Department of Pediatrics, Division of NeonatologyUniversity of Texas Health Science Center at San Antonio San Antonio Texas

2. The Chromosome 18 Registry and Research Society San Antonio Texas

3. Department of Pediatrics, Chromosome 18 Clinical Research CenterUniversity of Texas Health Science Center at San Antonio San Antonio Texas

4. Department of Medicine, Division of EndocrinologyUniversity of Texas Health‐San Antonio San Antonio Texas

5. Department of Pediatrics, Division of EndocrinologyPenn State Milton S. Hershey Medical Center Hershey Pennsylvania

Funder

National Institutes of Health

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61005

Reference20 articles.

1. Vitamin D: Deficiency, Sufficiency and Toxicity

2. Tetrasomy 18p: case report and review of literature

3. Adolescent Idiopathic Scoliosis and Osteopenia;Chiru M.;Mædica,2011

4. Clinician’s Guide to Prevention and Treatment of Osteoporosis

5. Serum alkaline phosphatase: normal values by sex and age.

Cited by 3 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. Phenotypic and cytogenetic features of an Iranian child with tetrasomy 18p syndrome: A case report;World Journal of Medical Genetics;2023-03-10

2. Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report;Molecular Cytogenetics;2022-06-27

3. Tetrasomy 18p in one non-identical twin born to healthy parents: A case report;Meta Gene;2021-12

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