(Q49147108)

English

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

scientific article published in December 2000

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scholarly article

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13. (English)

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

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author name string

Smith M

1

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Filipek PA

2

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Wu C

3

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Bocian M

4

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Hakim S

5

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Modahl C

6

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Spence MA

7

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

publication date

1 December 2000

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

96

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

6

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

765-770

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor alpha gene to a novel transcribed locus

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Analysis of the growth and transformation suppressor domains of promyelocytic leukemia gene, PML.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

The acute promyelocytic leukaemia specific PML and PLZF proteins localize to adjacent and functionally distinct nuclear bodies

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Molecular cloning of hSLP-1, a novel human brain-specific member of the band 7/MEC-2 family similar to Caenorhabditis elegans UNC-24.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Autism in Angelman syndrome: a population-based study

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Genetic analysis of protein tyrosine phosphatases

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

The Caenorhabditis elegans behavioral gene unc-24 encodes a novel bipartite protein similar to both erythrocyte band 7.2 (stomatin) and nonspecific lipid transfer protein.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820001204%2996%3A6%3C765%3A%3AAID-AJMG13%3E3.0.CO%3B2-L

21 January 2018

Identifiers

10.1002/1096-8628(20001204)96:6<765::AID-AJMG13>3.0.CO;2-L

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/11121177

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