Three probands with autistic disorder and isodicentric chromosome 15. (Q33970872)

30 July 2017

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title

Three probands with autistic disorder and isodicentric chromosome 15. (English)

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30 July 2017

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Wolpert CM

1

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30 July 2017

Menold MM

2

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30 July 2017

Bass MP

3

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30 July 2017

Qumsiyeh MB

4

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30 July 2017

Donnelly SL

5

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30 July 2017

Ravan SA

6

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30 July 2017

Vance JM

7

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30 July 2017

Gilbert JR

8

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30 July 2017

Abramson RK

9

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30 July 2017

Wright HH

10

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Cuccaro ML

11

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Pericak-Vance MA

12

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30 July 2017

1 June 2000

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American Journal of Medical Genetics Part A

30 July 2017

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30 July 2017

96

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30 July 2017

3

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30 July 2017

365-372

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Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

30 July 2017

1 reference

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The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

21 January 2018

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Brief report: epidemiology of autism

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Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

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Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation

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Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

21 January 2018

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Autism associated with marker chromosome.

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A case of autism associated with partial tetrasomy 15.

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A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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21 January 2018

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Is Angelman syndrome an alternate result of del(15)(q11q13)?

21 January 2018

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Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

1 reference

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

21 January 2018

1 reference

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Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

21 January 2018

1 reference

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Hypomelanosis of ITO. A study of 76 infantile cases.

21 January 2018

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Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

21 January 2018

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Concordance for the syndrome of autism in 40 pairs of afflicted twins

21 January 2018

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Oculocutaneous albinism and mental disorder. A report of two autistic boys

21 January 2018

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Genetic factors in child psychiatric disorders--I. A review of research strategies

21 January 2018

1 reference

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Genetic factors in child psychiatric disorders--II. Empirical findings

21 January 2018

1 reference

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Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

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Autism and genetics. A decade of research

21 January 2018

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A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

21 January 2018

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Autism in Angelman syndrome: a population-based study

21 January 2018

1 reference

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Behaviour problems in Angelman syndrome

21 January 2018

1 reference

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A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.

21 January 2018

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Polygenic disease: methods for mapping complex disease traits

21 January 2018

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Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

21 January 2018

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Cytogenetic and clinical studies in five cases of inv dup(15)

21 January 2018

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10.1002/1096-8628(20000612)96:3<365::AID-AJMG25>3.0.CO;2-X

21 January 2018

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1 reference

30 July 2017

1 reference