Literature DB >> 9550366

The 4q-syndrome: delineation of the minimal critical region to within band 4q31.

S P Robertson1, K O'Day, A Bankier.   

Abstract

A consistent phenotype has been associated with deletion of the distal long arm of chromosome 4. An invariant requirement for the phenotype in cases described so far has been the deletion of material from within band 4q31 but few other cases have been described that further aid the delineation of the minimum critical region sufficient for the expression of the phenotype. We report a child with a small interstitial deletion within band 4q31 who exhibits most of the features of the established 4q-phenotype.

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Year:  1998        PMID: 9550366     DOI: 10.1034/j.1399-0004.1998.531530114.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  5 in total

1.  4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Authors:  Goran Cuturilo; Björn Menten; Aleksandar Krstic; Danijela Drakulic; Ida Jovanovic; Vojislav Parezanovic; Milena Stevanovic
Journal:  Eur J Pediatr       Date:  2011-07-22       Impact factor: 3.183

2.  Interstitial 4q Deletion Syndrome Including NR3C2 Causing Pseudohypoaldosteronism.

Authors:  Amanda Barone Pritchard; Alyssa Ritter; Hutton M Kearney; Kosuke Izumi
Journal:  Mol Syndromol       Date:  2019-12-21

Review 3.  Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Authors:  Michael R Rossi; Miriam S DiMaio; Bixia Xiang; Kangmo Lu; Hande Kaymakcalan; Margretta Seashore; Maurice J Mahoney; Peining Li
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

4.  Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.

Authors:  Eric Scott Sills; M J Burns; Laurinda D Parker; Lisa P Carroll; Lisa L Kephart; C S Dyer; Peter R Papenhausen; Jessica G Davis
Journal:  Orphanet J Rare Dis       Date:  2007-02-12       Impact factor: 4.123

5.  Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3).

Authors:  Norma Elena de León Ojeda; Michel Soriano-Torres; Mercedes J Cabrera; Dunia Bárbara Benítez Ramos
Journal:  Case Rep Genet       Date:  2012-12-25
  5 in total

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