Literature DB >> 2964777

On the origin of chromosome anomaly.

R E Magenis1.   

Abstract

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Mesh：

Year:  1988        PMID： 2964777      PMCID： PMC1715222     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  40 in total

1.  Origin of the extra chromosome in trisomy 21.

Authors:  J F Mattei; M G Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132

2.  Trisomy 21: origin of non-disjunction.

Authors:  J del Mazo; A Pérez Castillo; J A Abrisqueta
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism.

Authors:  E B Hook; D Warburton
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families.

Authors:  M Mikkelsen; H Poulsen; J Grinsted; A Lange
Journal:  Ann Hum Genet       Date:  1980-07       Impact factor: 1.670

5.  Parental origin of chromosomes in Down's syndrome.

Authors:  C H Manning; H O Goodman
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Maternal age and origin of non-disjunction in trisomy 21.

Authors:  J F Mattei; S Ayme; M G Mattei; F Giraud
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

7.  Parental alpha 1-antitrypsin (PI) types and meiotic nondisjunction in the aetiology of Down syndrome.

Authors:  P H Jongbloet; R R Frants; A J Hamers
Journal:  Clin Genet       Date:  1981-10       Impact factor: 4.438

8.  Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study.

Authors:  P H Jongbloet; A Mulder; A J Hamers
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  The origin of human trisomy: a study of heteromorphisms and satellite associations.

Authors:  P A Jacobs; M Mayer
Journal:  Ann Hum Genet       Date:  1981-10       Impact factor: 1.670

10.  Dermatoglyphic and cytogenetic studies in parents of children with trisomy 21.

Authors:  R Schmidt; H Dar; H M Nitowsky
Journal:  Clin Genet       Date:  1981-09       Impact factor: 4.438
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  5 in total

1.  Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.

Authors:  H X Deng; K Abe; I Kondo; M Tsukahara; H Inagaki; I Hamada; Y Fukushima; N Niikawa
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

2.  Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man.

Authors:  N Simon Thomas; Miranda Durkie; Berendine Van Zyl; Richard Sanford; Gemma Potts; Sheila Youings; Nicholas Dennis; Patricia Jacobs
Journal:  Hum Genet       Date:  2006-02-22       Impact factor: 4.132

Review 3.  Cytogenetics of human spermatozoa: what about the reproductive relevance of structural chromosome aberrations?

Authors:  B E Rosenbusch
Journal:  J Assist Reprod Genet       Date:  1995-07       Impact factor: 3.412

4.  Frequency of XY sperm increases with age in fathers of boys with Klinefelter syndrome.

Authors:  X Lowe; B Eskenazi; D O Nelson; S Kidd; A Alme; A J Wyrobek
Journal:  Am J Hum Genet       Date:  2001-10-01       Impact factor: 11.025

5.  Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q.

Authors:  S B Cassidy; A J Gainey; M G Butler
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025
  5 in total

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