Literature DB >> 1640436

A terminal deletion of 11q.

C Schwarz1, C Mpofu, J E Wraith.   

Abstract

Mesh：

Year:  1992        PMID： 1640436      PMCID： PMC1016034     

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


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  3 in total

1.  [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].

Authors:  C Laurent; M C Biemont; M Veyron; J Guilhot; P Guibaud
Journal:  Ann Genet       Date:  1979

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

Authors:  A E O'Hare; E Grace; A T Edmunds
Journal:  Clin Genet       Date:  1984-04       Impact factor: 4.438

3.  New anomalies found in the 11q-syndrome.

Authors:  L Sirota; F Shabtai; I Landman; I Halbrecht; F Dulitzky
Journal:  Clin Genet       Date:  1984-12       Impact factor: 4.438
  3 in total
  1 in total

Review 1.  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
  1 in total

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