Literature DB >> 1583662

Monosomy 10qter: a new case.

M Teyssier1, C Charrin, J Dutruge, C Rousselle.   

Abstract

A new case of terminal deletion 10q26-qter is described. The phenotypic features are compatible with those of the previously reported cases. Deafness is reported for the first time.

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Mesh：

Year:  1992        PMID： 1583662      PMCID： PMC1015956          DOI： 10.1136/jmg.29.5.342

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


  5 in total

Review 1.  Terminal deletion of the long arm of chromosome 10: case report and review of the literature.

Authors:  M Gorinati; G Zamboni; N Padoin; A Dodero; D Caufin; L Memo
Journal:  Am J Med Genet       Date:  1989-08

2.  Post-mortem studies on two patients with 1-2 band cytogenetic deletions: 10q26----qter and r(9)(p24q34).

Authors:  A Smith; W A Evans; H Woolnough
Journal:  Ann Genet       Date:  1989

3.  Behaviour disorder in monosomy 10qter.

Authors:  L Mehta; D P Duckett; I D Young
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

4.  Deletions of the long arm of chromosome 10.

Authors:  S D Shapiro; K L Hansen; L M Pasztor; J H DiLiberti; R J Jorgenson; R S Young; C M Moore
Journal:  Am J Med Genet       Date:  1985-01

Review 5.  [Partial deletion 10qter. A new case].

Authors:  P Vanlieferinghen; P Dechelotte; F Charbonné
Journal:  Ann Genet       Date:  1987
  5 in total
  1 in total

1.  Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.

Authors:  Nathaniel D Miller; Melonie A Nance; Elizabeth S Wohler; Julie E Hoover-Fong; Emily Lisi; George H Thomas; Jonathan Pevsner
Journal:  Am J Med Genet A       Date:  2009-02-15       Impact factor: 2.802
  1 in total

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