Literature DB >> 5309411

Familial 18 q- syndrome.

E M Law, J G Masterson.   

Abstract

Mesh：

Year:  1969        PMID： 5309411

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


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  10 in total

1.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding technique.

Authors:  W L Gouw; L P ten Kate; G J Anders; A Okken
Journal:  Humangenetik       Date:  1973

6.  Familial occurrence of 18q.

Authors:  I Subrt; J Pokorný
Journal:  Humangenetik       Date:  1970-09-17

7.  Adults with Chromosome 18 Abnormalities.

Authors:  Bridgette Soileau; Minire Hasi; Courtney Sebold; Annice Hill; Louise O'Donnell; Daniel E Hale; Jannine D Cody
Journal:  J Genet Couns       Date:  2014-11-19       Impact factor: 2.537

Review 8.  Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Authors:  A D Kline; M E White; R Wapner; K Rojas; L G Biesecker; J Kamholz; E H Zackai; M Muenke; C I Scott; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

9.  The malformations of the urinary system in autosomal disorders.

Authors:  G I Kravtzova; G I Lazjuk; I W Lurie
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1975-10-20

10.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975
  10 in total

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