Literature DB >> 1262237

A bisatellited marker chromosome in a mentally retarded girl with infantile autism.

K Rasmussen, J Nielsen, I Sillesen, B H Brask, P Saldaña-Garcia.   

Abstract

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Year:  1976        PMID： 1262237     DOI： 10.1111/j.1601-5223.1976.tb01535.x

Source DB:  PubMed          Journal:  Hereditas        ISSN： 0018-0661            Impact factor:   3.271


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  5 in total

1.  Prenatal detection of an accessory chromosome identified as an inversion duplication (15).

Authors:  G Stetten; B Sroka-Zaczek; V L Corson
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

Review 3.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  A case report of an autistic girl with an extra bisatellited marker chromosome.

Authors:  A Hansen; B H Brask; J Nielsen; K Rasmussen; I Sillesen
Journal:  J Autism Child Schizophr       Date:  1977-09

5.  Brief report: a case of chromosome 22 alteration associated with autistic syndrome.

Authors:  F B Assumpcão Júnior
Journal:  J Autism Dev Disord       Date:  1998-06
  5 in total

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