Literature DB >> 6713716

Deletion of the long arm of chromosome 11 [46,XX,del(11)(q24.1--qter)].

A E O'Hare, E Grace, A T Edmunds.   

Abstract

A child who presented at three months of age with pyloric stenosis and pancytopenia was found to have a partial deletion of the long arm of chromosome 11, del(11)(q24.1----qter). Only two previous cases have been described with an apparently identical chromosomal deletion, and both exhibit similar phenotypic features. Other patients with larger deletions of the distal region of the long arm of chromosome 11 show many features in common with these three cases. It is suggested that the region of the long arm of chromosome 11 from band q24.1 to qter may contain the genetic material responsible for the expression of the 11q - phenotype.

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Year:  1984        PMID: 6713716     DOI: 10.1111/j.1399-0004.1984.tb02007.x

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


  8 in total

1.  A terminal deletion of 11q.

Authors:  C Schwarz; C Mpofu; J E Wraith
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

2.  Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter).

Authors:  T Arinami; T Hirano; K Kobayashi; Y Yamanouchi; H Hamaguchi
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

3.  Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.

Authors:  C P Chen; F F Liu; S W Jan; C P Chen; C C Lan
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

4.  Congenital ocular and other systemic abnormalities associated with ring-11 chromosome.

Authors:  S Daniele; F Pecorelli; L Tiepolo; R Armellini; F S Liotti
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1986       Impact factor: 3.117

5.  Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomalies.

Authors:  S A al-Awadi; K K Naguib; S A al-Othman; T S Sundareshan
Journal:  Indian J Pediatr       Date:  1988 Mar-Apr       Impact factor: 1.967

Review 6.  Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors:  E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

7.  Report of a deletion 11 (qter----q23.3) and short review of the literature.

Authors:  W Küster; H J Gebauer; F Majewski; H G Lenard
Journal:  Eur J Pediatr       Date:  1985-09       Impact factor: 3.183

8.  Clinical and molecular characterization of patients with distal 11q deletions.

Authors:  L A Penny; M Dell'Aquila; M C Jones; J Bergoffen; C Cunniff; J P Fryns; E Grace; J M Graham; B Kousseff; T Mattina
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

  8 in total

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