Literature DB >> 6862443

Confirmation of a de novo duplication, dup(10)(q24 leads to q26), by GOT1 gene dosage studies.

D J Tomkins, B J Gitelman, M H Roberts.   

Abstract

A girl with mental retardation and the facies associated with the distal 10q duplication syndrome was found to have a tandem duplication of 10q24 to 10q26. This was confirmed by gene dosage studies of glutamic oxaloacetic transaminase 1. The clinical features of this patient are compared with those of other reported cases of the distal 10q duplication syndrome with duplication-deficiency karyotypes due to familial reciprocal translocations or inversions or with tandem duplication of a more proximal region of 10q. Reports of tandem duplications in man and possible mechanisms of origin are discussed.

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Year:  1983        PMID: 6862443     DOI: 10.1007/bf00274764

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


  14 in total

1.  [Phenotypic variation in partial trisomy 4q (author's transl)].

Authors:  W Vogel; J W Siebers; J Gunkel
Journal:  Humangenetik       Date:  1975-06-19

2.  Methods for the estimation of three vitamin dependent red cell enzymes.

Authors:  D G Williams
Journal:  Clin Biochem       Date:  1976-12       Impact factor: 3.281

3.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

4.  [Partial "de novo" trisomy 10q (author's transl)].

Authors:  R Berger; J Derre; M Murawsky; C Amiel-Tison
Journal:  J Genet Hum       Date:  1976-12

5.  Partial 4q trisomy. Apropos of 3 cases.

Authors:  B Dutrillaux; C Laurent; A Forabosco; B Noel; E Suerinc; M C Biemont; J B Cotton
Journal:  Ann Genet       Date:  1975-03

6.  Gene dosage effect: intraband mapping of human soluble glutamic oxaloacetic transaminase.

Authors:  R A Spritz; B S Emanuel; C J Chern; W J Mellman
Journal:  Cytogenet Cell Genet       Date:  1979

7.  Two cases of partial trisomy 10q in the same family caused by parental direct insertion [ins. (15;10) (q15;q24q26)].

Authors:  E Back; J Kosmützky; A Schuwald; H Hameister
Journal:  Ann Genet       Date:  1979

8.  Serial duplication of 10 (q11 leads to q22) in a patient with minor congenital malformations.

Authors:  W Vogel; E Back; W Imm
Journal:  Clin Genet       Date:  1978-02       Impact factor: 4.438

9.  Serial duplication of 10 (q21 to q22) in a mentally retarded boy with congenital malformations.

Authors:  M Koivisto; R Herva; S L Linna
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Report of the committee on the genetic constitution of chromosomes 10, 11, and 12. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping.

Authors:  P S Gerald; O J Miller
Journal:  Cytogenet Cell Genet       Date:  1982
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