Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02923.x/fullpdf
Reference12 articles.
1. The Prader-Willi syndrome: a study of 40 patients and a review of the literature;Bray;Medicine,1983
2. Clinical and cytogenetic survey of 39 individuals with Prader-Willi syndrome;Butler;Am. J. Med. Genet.,1986
3. Low recurrence risk for Prader-Willi syndrome (letter);Cassidy;Am. J. Med. Genet.,1987
4. Neonatal diagnosis of Prader-Willi syndrome and its implications;Greenberg;Am. J. Med. Genet.,1987
5. Deletions of proximal 15q without Prader-Willi syndrome;Greenberg;Am. J. Med. Genet.,1987
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1. Perinatal dyskinesia as a presenting feature in Prader Willi Syndrome;European Journal of Paediatric Neurology;2009-07
2. Strength characterization of knee flexor and extensor muscles in Prader-Willi and obese patients;BMC Musculoskeletal Disorders;2009-05-06
3. The Prader–Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation;Differentiation;2008-11
4. Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects;Clinical Genetics;2008-06-28
5. Pre-, peri- and postnatal complications in Prader–Willi syndrome in a UK sample;Early Human Development;2008-05
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