Literature DB >> 3169750

Deletion 11q23.3 without familial predisposition.

C Hausmann, E Back, G Wolff, I Voiculescu.   

Abstract

Mesh:

Year:  1988        PMID: 3169750     DOI: 10.1007/bf00702875

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


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  4 in total

1.  Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.

Authors:  L E Voullaire; G C Webb; M A Leversha
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

2.  Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use.

Authors:  E B Hook
Journal:  Am J Hum Genet       Date:  1977-01       Impact factor: 11.025

3.  Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1.

Authors:  J P Fryns; A Kleczkowska; M Buttiens; P Marien; H van den Berghe
Journal:  Clin Genet       Date:  1986-10       Impact factor: 4.438

4.  Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding.

Authors:  C Tengström; S Autio
Journal:  Clin Genet       Date:  1987-01       Impact factor: 4.438

  4 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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