Diagnosing Prader-Willi syndrome-Reference-Cited by-同舟云学术

Diagnosing Prader-Willi syndrome

Published:1995-06 Issue:8965 Volume:345 Page:1590
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Young I.D.

Publisher

Elsevier BV

Subject

General Medicine

Reference11 articles.

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2. Ein syndrom von Adipositas, Kleinwuchs, Kryptorchidismus und Oligophrenie nach Myatonieartigem Zustand im Neugeborenalter;Prader;Schweiz Med Wschr,1956

3. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndrome;Nicholls;Am J Med Genet,1993

4. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region;Özçelik;Nature Genet,1992

5. Molecular diagnosis of the Prader-Willi and Angelman syndrome by detection of parent-of-origin specific DNA methylation in 15q11-13;Dittrich;Hum Genet,1992

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1. DNA Methylation as a Biomarker for Neuropsychiatric Diseases;International Journal of Neuroscience;2012-01-05

2. Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader–Willi syndrome;Clinical Endocrinology;2008-06

3. The challenge of follow-up in narrowband ultraviolet B phototherapy;British Journal of Dermatology;2007-08

4. Inhibition of T helper 2 chemokine production by narrowband ultraviolet B in cultured keratinocytes;British Journal of Dermatology;2007-05

5. Adiponectin Levels in Prepubertal Children with Prader-Willi Syndrome before and during Growth Hormone Therapy;The Journal of Clinical Endocrinology & Metabolism;2007-04-01