Literature DB >> 134160

Chromosome survey of total population of mentally subnormal in North-East of Scotland.

R M Speed, A W Johnston, H J Evans.   

Abstract

A cytogenetic survey of the complete population of mentally subnormal in the North-East of Scotland has been undertaken. A register for the mentally subnormal within the region already existed, and all persons recorded, whether they resided at home or in subnormality hospitals or other institutional care, were included. The total number recorded was 3020 and of these 2770 were examined cytologically. In all 297 (10.7%) were shown to have a chromosomal abnormality, and of these Down's syndrome accounted for 250 (9%). Within this category was an unexpected excess of males. Deletions and supernumeraries comprised the remaining autosomal anomalies. Increased numbers of sex chromosome abnormalities among high grade mentally subnormal individuals were confirmed for both sexes. The survey has shown that abnormal chromosome complements contribute significantly to the causation of mental retardation, and has also provided estimates which cannot be obtained from hospital surveys alone.

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Year:  1976        PMID: 134160      PMCID: PMC1013419          DOI: 10.1136/jmg.13.4.295

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  43 in total

1.  TWELVE UNRELATED TRANSLOCATION MONGOLS: CYTOGENETIC, GENETIC AND PARENTAL AGE DATA.

Authors:  F R SERGOVICH; H C SOLTAN; D H CARR
Journal:  Cytogenetics       Date:  1964

2.  CLINICAL AND CYTOGENETIC STUDIES ON A GROUP OF FEMALES WITH XXX SEX CHROMOSOME COMPLEMENTS.

Authors:  R W DAY; W LARSON; S W WRIGHT
Journal:  J Pediatr       Date:  1964-01       Impact factor: 4.406

3.  A CYTOGENETIC AND STATISTICAL SURVEY OF 105 CASES OF MONGOLISM.

Authors:  R G CHITHAM; E MACIVER
Journal:  Ann Hum Genet       Date:  1965-03       Impact factor: 1.670

4.  MORTALITY IN PATIENTS WITH DOWN'S SYNDROME.

Authors:  H FORSSMAN; H O AKESSON
Journal:  J Ment Defic Res       Date:  1965-06

5.  CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA.

Authors:  G SCHACHENMANN; W SCHMID; M FRACCARO; A MANNINI; L TIEPOLO; G P PERONA; E SARTORI
Journal:  Lancet       Date:  1965-08-07       Impact factor: 79.321

6.  Incidence, mortality, and dex distribution of mongoloid defectives.

Authors:  R G RECORD; A SMITH
Journal:  Br J Prev Soc Med       Date:  1955-01

7.  Data on mongolism in Victoria, Australia: prevalence and life expectation.

Authors:  R D COLLMANN; A STOLLER
Journal:  J Ment Defic Res       Date:  1963-06

8.  Mosaicism in a mother with a mongol child.

Authors:  C E BLANK; E GEMMELL; M D CASEY; M LORD
Journal:  Br Med J       Date:  1962-08-11

9.  Smears from the oral mucosa in the detection of chromosomal sex.

Authors:  K L MOORE; M L BARR
Journal:  Lancet       Date:  1955-07-09       Impact factor: 79.321

10.  Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome.

Authors:  S Kaffe; L Y Hsu; K Hirschhorn
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

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  17 in total

1.  Chromosome studies of males in an institution for the mentally handicapped.

Authors:  C J English; E V Davison; M S Bhate; L Barrett
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

2.  Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

Authors:  R Plattner; N A Heerema; S R Patil; P N Howard-Peebles; C G Palmer
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

3.  The genetic significance of accessory bisatellited marker chromosomes.

Authors:  P Steinbach; M Djalali; I Hansmann; E Kattner; M Meisel-Stosiek; H D Probeck; A Schmidt; M Wolf
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome.

Authors:  P A Jacobs; M Mayer; J Matsuura; F Rhoads; S C Yee
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Reciprocal translocation t(5;6)(p13;q27) through three generations: case report of cri du chat syndrome.

Authors:  T Hashimoto; R Tsukino; H Chiyo; J Furuyama
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

6.  Antenatal diagnosis of a de novo reciprocal translocation 46,XX,t(3;7)(q21;q11).

Authors:  P Husslein; W Schnedl; P Wagenbichler
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

7.  Chromosome survey of total population of mentally subnormal in North-East Scotland.

Authors:  D P Forster
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318

8.  Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.

Authors:  M G Butler; D N Singh
Journal:  J Intellect Disabil Res       Date:  1993-04

9.  A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors:  A Smith; M Noel
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.

Authors:  I Tierney; D Axworthy; L Smith; S G Ratcliffe
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

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