Literature DB >> 6036276

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

A De Capoa, D Warburton, W R Breg, D A Miller, O J Miller.   

Abstract

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Year:  1967        PMID： 6036276      PMCID： PMC1706310     

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


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  7 in total

1.  A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Authors:  K H GUSTAVSON; S C FINLEY; W H FINLEY; B JALLING
Journal:  Acta Paediatr       Date:  1964-03       Impact factor: 2.299

2.  [5-21-22 translocation and the crying cat syndrome].

Authors:  J de Grouchy; J C Gabilan
Journal:  Ann Genet       Date:  1965

3.  [The crying cat syndrome and its reciprocal].

Authors:  J Lejeune; J Lafourcade; R Berger; M O Rethoré
Journal:  Ann Genet       Date:  1965

4.  [The deletion of the short arms of a group 4-5 chromosome. Study of a case].

Authors:  L Koulischer; C Quersin
Journal:  Acta Paediatr Belg       Date:  1965

5.  Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms.

Authors:  D Warburton; D A Miller; O J Miller; W R Breg; A De Capoa; M W Shaw
Journal:  Am J Hum Genet       Date:  1967-05       Impact factor: 11.025

6.  [Crying cat syndrome with translocation 5/D 2].

Authors:  U Wolf; H Reinwein; W Gey; J Klose
Journal:  Humangenetik       Date:  1966

7.  Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.

Authors:  O J Miller; W R Breg; D Warburton; D A Miller; I L Firschein; K Hirschhorn
Journal:  Cytogenetics       Date:  1966
  7 in total
  22 in total

1.  A family with an inherited translocation involving the no. 4/no. 21 chromosomes.

Authors:  J M Darmady; M Seabright
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

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

Authors:  R M Speed; A W Johnston; H J Evans
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

3.  'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.

Authors:  F S Brimblecombe; F J Lewis; M Vowles
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  "Complete" trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p. Case report and review of the literature.

Authors:  N J Leschot; K S Lim
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

6.  Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

Authors:  L Owen; B Martin; C E Blank; F Harris
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

7.  Annotation: genetic effects of aneuploidy.

Authors:  L Sandler; F Hecht
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

8.  Transmission of the cri-du-chat syndrome from a maternal balanced translocation carrier, t(5p-;11q+).

Authors:  D N Singh; R A Osborne; R A Wiscovitch
Journal:  Humangenetik       Date:  1973-12-20

9.  Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.

Authors:  W L Gouw; G J Anders; L P ten Kate; C J de Groot
Journal:  Humangenetik       Date:  1972

10.  Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

Authors:  H Schröchsnadel; C Feichtinger; C Scheminzky
Journal:  Humangenetik       Date:  1975-10-07
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