Literature DB >> 6500580

Origin of extra chromosome in Patau syndrome.

S Ishikiriyama, N Niikawa.   

Abstract

Five live-born infants with Patau syndrome were studied for the nondisjunctional origin of the extra chromosome. Transmission modes of chromosomes 13 from parents to a child were determined using both QFQ- and RFA-heteromorphisms as markers, and the origin was ascertained in all of the patients. The extra chromosome had originated in nondisjunction at the maternal first meiotic division in two patients, at the maternal second meiosis in other two, and at the paternal first meiosis in the remaining one. Summarizing the results of the present study, together with those of the previous studies on a liveborn and abortuses with trisomy 13, nondisjunction at the maternal and the paternal meiosis occurred in this trisomy in the ratio of 14:3. This ratio is not statistically different from that inferred from the previous studies for Down syndrome. These findings suggest that there may be a fundamental mechanism common to the occurrence of nondisjunction in the acrocentric trisomies.

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Year:  1984        PMID: 6500580     DOI: 10.1007/bf00418400

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  Aetiology of spontaneous abortion. A cytogenetic and epidemiological study of 288 abortuses and their parents.

Authors:  J G Lauritsen
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1976

2.  Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

Authors:  R C Juberg; P N Mowrey
Journal:  Am J Med Genet       Date:  1983-09

3.  A cytogenetic study of 1000 spontaneous abortions.

Authors:  T Hassold; N Chen; J Funkhouser; T Jooss; B Manuel; J Matsuura; A Matsuyama; C Wilson; J A Yamane; P A Jacobs
Journal:  Ann Hum Genet       Date:  1980-10       Impact factor: 1.670

4.  Anatomic and chromosomal anomalies in 639 spontaneous abortuses.

Authors:  T Kajii; A Ferrier; N Niikawa; H Takahara; K Ohama; S Avirachan
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Parental origin of triploidy and D and G trisomy in spontaneous abortions.

Authors:  B G Brennan; D H Carr
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

6.  Origin of acrocentric trisomies in spontaneous abortuses.

Authors:  N Niikawa; E Merotto; T Kajii
Journal:  Hum Genet       Date:  1977-12-29       Impact factor: 4.132

7.  Sequential Q- and Acridine orange-marker technique.

Authors:  N Niikawa; T Kajii
Journal:  Humangenetik       Date:  1975-10-20

8.  Parental origin of chromosome abnormalities in spontaneous abortions.

Authors:  G H Meulenbroek; J P Geraedts
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438

  9 in total
  6 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.  Frequency and distribution of aneuploidy in human female gametes.

Authors:  F Pellestor
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

3.  Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphism.

Authors:  T Kondoh; H Tonoki; T Matsumoto; M Tsukahara; N Niikawa
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

4.  Parental origin of the extra chromosome in trisomy 18.

Authors:  K G Kupke; U Müller
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

5.  Cytogenetic and molecular studies of trisomy 13.

Authors:  T Hassold; P A Jacobs; M Leppert; M Sheldon
Journal:  J Med Genet       Date:  1987-12       Impact factor: 6.318

6.  Overexpression of esterase D in kidney from trisomy 13 fetuses.

Authors:  S Loughna; P Bennett; G Gau; K Nicolaides; S Blunt; G Moore
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

  6 in total

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