Genetics of Prader—Willi Syndrome-Reference-Cited by-同舟云学术

Genetics of Prader—Willi Syndrome

Published:1995 Issue: Volume: Page:18-31
ISSN:
Container-title:Management of Prader-Willi Syndrome
language:
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Author:

Cassidy Suzanne B.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4615-7384-5_2.pdf

Reference14 articles.

1. Angelman, H. (1965). “Puppet” children: A report on three cases. Developmental Medicine and Child Neurology, 7, 681–683.

2. Butler, M.G. (1990). Prader-Willi syndrome: Current understanding of cause and diagnosis. American Journal of Genetics, 35, 319–332.

3. Butler, M.G., & Palmar, C.G. (1983). Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet, 1, 285–286.

4. Cassidy, S.B., Lai, L.W., Erickson, R.P., Magnuson, I., Thomas, E., Gendron, R., & Herrmann, J. (1992). Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. American Journal of Human Genetics, 51, 701–708.

5. Clayton-Smith, J., & Pembrey, M.E. (1992). Angelman syndrome. Journal of Medical Genetics, 29, 412–415.

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1. Hypogonadism and pubertal development in Prader-Willi syndrome;European Journal of Pediatrics;2003-02-27

2. Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome;Mental Retardation and Developmental Disabilities Research Reviews;1999

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4. Prader-Willi Syndrome: Genetic, Behavioral, and Treatment Issues;Child and Adolescent Psychiatric Clinics of North America;1996-10