Literature DB >> 5303425

[46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].

J de Grouchy, F Lautmann.   

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Year:  1968        PMID： 5303425

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  10 in total

1.  Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1.

Authors:  H N Bass; R S Sparkes
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

2.  Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.

Authors:  C G Palmer; C Poland; T Reed; J Kojetin
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

Review 3.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

Review 4.  Are double translocations double trouble?

Authors:  S M Bowser-Riley; M J Griffiths; M R Creasy; P A Farndon; K E Martin; D A Thomson; S A Larkins; R A Johnson; J L Watt
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

5.  Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Authors:  H Van den Berghe; M Van Eygen; J P Fryns; W Tanghe; H Verresen
Journal:  Humangenetik       Date:  1973-05-25

6.  Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.

Authors:  P Genest; R Lachance; J Poty; D Jacob
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

7.  Segregation of two independent chromosomal translocations in one family.

Authors:  K Miller; S D Flatz
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  A malformed baby with two separate de novo translocations.

Authors:  W E Chewings; T P Cocks; R J Gardner; J E Clarkson
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

9.  Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.

Authors:  J B Bijlsma; H F de France; L M Bleeker-Wagemakers; P F Dijkstra
Journal:  Hum Genet       Date:  1978-01-19       Impact factor: 4.132

10.  A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.

Authors:  G Simoni; E Montali; F Rossella; L Dalprà; F Lo Curto
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132
  10 in total

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