Absence of linkage and linkage disequilibrium to chromosome 15q11‐q13 markers in 139 multiplex families with autism-Reference-Cited by-同舟云学术

Absence of linkage and linkage disequilibrium to chromosome 15q11‐q13 markers in 139 multiplex families with autism

Published:1999-10-15 Issue:5 Volume:88 Page:551-556
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Salmon Boyd¹,Hallmayer Joachim¹,Rogers Tamara²,Kalaydjieva Luba²,Petersen P. Brent³,Nicholas Peter³,Pingree Carmen³,McMahon William³,Spiker Donna⁴,Lotspeich Linda⁴,Kraemer Helena⁴,McCague Patty⁴,Dimiceli Sue⁴,Nouri Nassim⁵,Pitts Tawna⁵,Yang Joan⁵,Hinds David⁵,Myers Richard M.⁵,Risch Neil⁵

Affiliation:

1. Centre for Clinical Research in Neuropsychiatry, Graylands Hospital/University of Western Australia, Perth, Australia

2. Centre for Human Genetics, Edith Cowan University, Perth, Australia

3. Department of Psychiatry, University of Utah, Salt Lake City, Utah

4. Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California

5. Department of Genetics, Stanford University School of Medicine, Stanford, California

Publisher

Wiley

Subject

Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/%28SICI%291096-8628%2819991015%2988%3A5%3C551%3A%3AAID-AJMG21%3E3.0.CO%3B2-%23

Reference36 articles.

1. Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism

2. Autism as a strongly genetic disorder: evidence from a British twin study

3. Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder

4. Duplication of the 15q11-13 Region in a Patient with Autism, Epilepsy and Ataxia

5. Molecular characterization of two proximal deletion breakpoint regions in Both Prader‐Willi and Angelman syndrome patients;Christian SL;Am J Hum Genet,1995

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