Severe short stature and Wolf-Hirschhorn syndrome: response to growth hormone in two cases without growth hormone deficiency
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Embryology,Anatomy
Link
http://academic.oup.com/omcr/article-pdf/2015/2/211/4218677/omv008.pdf
Reference11 articles.
1. An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality
2. Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2
3. Wolf–Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage
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1. The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapy;BMC Medical Genomics;2020-12
2. Hip displacement in Wolf–Hirschhorn syndrome: Report on three cases and review of associated musculoskeletal pathologies;American Journal of Medical Genetics Part A;2020-04-07
3. Growth trajectory and pubertal tempo from birth till final height in a girl with Wolf-Hirschhorn syndrome;Endocrinology, Diabetes & Metabolism Case Reports;2018-04-12
4. An examination of the effects of different doses of recombinant human growth hormone on children with growth hormone deficiency;Experimental and Therapeutic Medicine;2016-02-19
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