Literature DB >> 7682619

Interstitial deletion of chromosome 10q23: a new case and review.

S A Farrell1, W Szymonowicz, G Chow, A M Summers.   

Abstract

A new case of a deletion of 10q23 is described. Only two other deletions involving this region have been previously noted. A review of clinical features of these three children did not show a distinct pattern of dysmorphic features. Other interstitial deletions of 10q are listed.

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Mesh：

Year:  1993        PMID： 7682619      PMCID： PMC1016310          DOI： 10.1136/jmg.30.3.248

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


  12 in total

Review 1.  Chromosome 10qter deletion syndrome: a review and report of three new cases.

Authors:  E A Wulfsberg; R P Weaver; C M Cunniff; M C Jones; K L Jones
Journal:  Am J Med Genet       Date:  1989-03

Review 2.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

3.  Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).

Authors:  J J Holden; E A MacDonald
Journal:  Am J Med Genet       Date:  1985-02

4.  De novo 10q23 interstitial deletion.

Authors:  M A Mori; F Gomez-Sabrido; A Diaz de Bustamante; I Pinel; M L Martinez-Frias
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

5.  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

6.  A case of interstitial deletion of 10q25.2----q26.1.

Authors:  D E Rooney; K Williams; D V Coleman; A Habel
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

7.  Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23).

Authors:  P Chieri; N Iölster
Journal:  Clin Genet       Date:  1983-08       Impact factor: 4.438

Review 8.  Interstitial deletion of 10q: clinical features and literature review.

Authors:  S Lobo; J Cervenka; A London; M E Pierpont
Journal:  Am J Med Genet       Date:  1992-07-01

9.  Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).

Authors:  M J van de Vooren; H T Planteydt; A Hagemeijer; M F Peters-Slough; M J Timmerman
Journal:  Clin Genet       Date:  1984-01       Impact factor: 4.438

10.  Interstitial deletion of the long arm of chromosome 10.

Authors:  M Ray; A G Hunter; K Josifek
Journal:  Ann Genet       Date:  1980
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  2 in total

1.  Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities.

Authors:  Jorune Balciuniene; Ningping Feng; Kelly Iyadurai; Betsy Hirsch; Lawrence Charnas; Brent R Bill; Mathew C Easterday; Johan Staaf; LeAnn Oseth; Desiree Czapansky-Beilman; Dimitri Avramopoulos; George H Thomas; Ake Borg; David Valle; Lisa A Schimmenti; Scott B Selleck
Journal:  Am J Hum Genet       Date:  2007-03-20       Impact factor: 11.025

2.  A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: a new patient with a novel feature.

Authors:  Piero Pavone; Andrea D Praticò; Corrado Campisi; Raffaele Falsaperla
Journal:  BMJ Case Rep       Date:  2016-04-18
  2 in total

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