Literature DB >> 317789

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

C Laurent, M C Biemont, M Veyron, J Guilhot, P Guibaud.   

Abstract

Mesh：

Year:  1979        PMID： 317789

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  2 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

Review 2.  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
  2 in total

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