Literature DB >> 5149534

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

P Genest, R Lachance, J Poty, D Jacob.   

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Year:  1971        PMID： 5149534      PMCID： PMC1469101          DOI： 10.1136/jmg.8.4.504

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  9 in total

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

Authors:  J de Grouchy; F Lautmann
Journal:  Ann Genet       Date:  1968-06

2.  A case of a balanced 2/D translocation.

Authors:  E Lisco; H Lisco
Journal:  Ann Genet       Date:  1967-03

3.  [Familial translocation 2-D].

Authors:  N Ricci; B Dallapiccola; G Cotti
Journal:  Ann Genet       Date:  1968-06

4.  A mentally retarded child convulsions, agenesis of the corpus callosum, and a translocation involving chromosomes 2 and the B group.

Authors:  D J Mantle; P Mitchell; K Kucheria; J Wilson
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

5.  MN blood-group locus: data concerning the possible chromosomal location.

Authors:  J German; M E Walker; F H Stiefel; F H Allen
Journal:  Science       Date:  1968-11-29       Impact factor: 47.728

6.  An unusual chromosome abnormality 2-D translocation.

Authors:  L E Reisman; S Kasahara
Journal:  Am J Dis Child       Date:  1968-05

7.  Congenital abnormalities in a child with presumptive karyotype 46. XX, t (2q-; 17q+).

Authors:  J Masterson; E Law; A MacDonald; D Donovan
Journal:  Ir J Med Sci       Date:  1970-01       Impact factor: 1.568

8.  t(2q-; Dq+) in a mentally retarded female child.

Authors:  B C Davison; J Bedford; W Dunn
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

9.  Placental chorangiomata and mental deficiency in a child with 2/15 translocation: 46,XX,t(2q-;15q+).

Authors:  D H Wurster; D Hoefnagel; K Benirschke; F H Allen
Journal:  Cytogenetics       Date:  1969
  9 in total
  3 in total

1.  Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.

Authors:  J F Mattei; M G Mattei; J Coignet; F Giraud
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

2.  Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).

Authors:  R S Young; S D Shapiro; K L Hansen; L K Hine; D E Rainosek; F A Guerra
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

3.  Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family.

Authors:  R B Levisky; A M Vianna-Morgante; O Frota-Pessoa; M Scaff; A M Tsanaclis; J A Levy
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318
  3 in total

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