Literature DB >> 7529320

An interstitial deletion of chromosome 7(q35).

K Fagan1, C Kennedy, L Roddick, A Colley.   

Abstract

We describe a patient with developmental delay, mild dysmorphic features, and monosomy of 7q35. Only one other patient with an interstitial deletion of this band has been previously reported. A review of clinical features of these two children did not show similarities in dysmorphic features. Reports of patients with other 7q interstitial deletions are listed.

Entities:  

Mesh：

Year:  1994        PMID： 7529320      PMCID： PMC1050089          DOI： 10.1136/jmg.31.9.738

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


  5 in total

Review 1.  The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report.

Authors:  R S Verma; R A Conte; S E Sayegh; D Kanjilal
Journal:  Clin Genet       Date:  1992-02       Impact factor: 4.438

2.  Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

Authors:  K B Nielsen; F Egede; I Mouridsen; J Mohr
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

3.  De novo 3q/7q translocation and associated interstitial 7q35 deletion.

Authors:  J P Fryns; A Kleczkowska; H van den Berghe
Journal:  Clin Genet       Date:  1988-01       Impact factor: 4.438

4.  Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7.

Authors:  M A Baeteman; N Philip; M G Mattei; J F Mattei
Journal:  Clin Genet       Date:  1985-06       Impact factor: 4.438

5.  A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.

Authors:  K Fagan; A Gill; R Henry; I Wilkinson; B Carey
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318
  5 in total
  3 in total

1.  Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome.

Authors:  Kristen Dilzell; Diana Darcy; John Sum; Robert Wallerstein
Journal:  Case Rep Genet       Date:  2015-05-03

2.  An Interstitial Deletion at 7q33-36.1 in a Patient with Intellectual Disability, Significant Language Delay, and Severe Microcephaly.

Authors:  Trupti Kale; Melissa Philip
Journal:  Case Rep Genet       Date:  2016-12-08

3.  Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C.

Authors:  Lucie Tosca; Loïc Drévillon; Aurélie Mouka; Laure Lecerf; Audrey Briand; Valérie Ortonne; Virginie Benoit; Sophie Brisset; Lionel Van Maldergem; Quitterie Laudouar; Solveig Heide; Michel Goossens; Irina Giurgea; Gérard Tachdjian; Corinne Métay
Journal:  Mol Genet Genomic Med       Date:  2021-09-28       Impact factor: 2.183
  3 in total

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