Literature DB >> 7327579

Complex balanced translocation of chromosomes 2, 3, and 13.

R S Muneer, D L Donaldson, O M Rennert.   

Abstract

Mesh：

Year:  1981        PMID： 7327579     DOI： 10.1007/bf00293074

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


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  9 in total

1.  De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.

Authors:  E C Jenkins; F M Curcuru-Giordano; S G Krishna; J Cantarella
Journal:  Ann Genet       Date:  1975-06

2.  Partial trisomy for different segments of chromosome 13 in several individuals of the same family.

Authors:  R S Wilroy; R L Summitt; P R Martens
Journal:  Birth Defects Orig Artic Ser       Date:  1975

3.  Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim.

Authors:  A Schinzel; W Schmid
Journal:  Humangenetik       Date:  1974

4.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

5.  Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.

Authors:  H J Kim; L Y Hsu; L C Goldsmith; L Strauss; K Hirschhorn
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

6.  Partial trisomy for the distal long arm of chromosome 13, 46,,XY. Repository identification No. GM-1663.

Authors:  A Schinzel; M M Aronson; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1979

7.  Rearrangements involving four chromosomes in a child with congenital abnormalities.

Authors:  M Seabright; N Gregson; E Pacifico; S Mould; J Ryde; J Pearson; A Bradley
Journal:  Cytogenet Cell Genet       Date:  1978

8.  A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion, del(14) (q13q22) in a child with congenital glaucoma and cleft lip and palate.

Authors:  P D Buchanan; K W Rao; C L Doerr; A S Aylsworth
Journal:  Birth Defects Orig Artic Ser       Date:  1978

9.  Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes.

Authors:  C Fonatsch; S D Flatz; E Weitzel
Journal:  Clin Genet       Date:  1979-02       Impact factor: 4.438
  9 in total
  5 in total

1.  Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes.

Authors:  Sulman Basit; Syed Kamran-ul-Hassan Naqvi; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2011-08-30       Impact factor: 4.132

2.  Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Authors:  M H Bogart; C L Bradshaw; O W Jones; J E Schanberger
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

3.  Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.

Authors:  S Walker; P J Howard; D Hunter
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

4.  The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Authors:  F Rivas; H Rivera; M L Plascencia; B Ibarra; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

Authors:  A Joseph; I M Thomas
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318
  5 in total

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