Literature DB >> 302679

Trigonocephaly and the 11q- syndrome.

S B Cassidy, R M Heller, A W Kilroy, W McKelvey, E Engel.   

Abstract

A seventh case of deletion of the distal long arm of a chromosome 11 is described. As in other cases with this karyotypic abnormality, trigonocephaly is the most noticeable phenotypic peculiarity. A review of common developmental and dysmorphic features among the seven recognized cases is presented.

Entities:  

Mesh：

Year:  1977        PMID： 302679

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


  7 in total

1.  Partial deletion of the long arm chromosome 11 in Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1986 Jan-Feb       Impact factor: 1.967

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

3.  Partial deletion of the long arm of chromosome 11 the Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1984 May-Jun       Impact factor: 1.967

4.  Absence of constitutive heterochromatin in a partially identified supernumerary marker chromosome.

Authors:  G S Pai; G H Thomas; P J Benke
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

5.  Partial monosomy 10p syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; F M Alkema
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

6.  Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

Authors:  A Schinzel; P Auf der Maur; H Moser
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

7.  Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

Authors:  B M Lippe; R S Sparkes; B Fass; L Neidengard
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318
  7 in total

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