Literature DB >> 5300122

[Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].

J Lejeune, R Berger, M O Réthoré, J Lafourcade, B Dutrillaux, P Canlorbe, B Labrune.   

Abstract

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Year:  1967        PMID： 5300122

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


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  11 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.  The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).

Authors:  C E Parker; J Mavalwala; R Koch; A Hatashita; A Derencsenyi
Journal:  Calif Med       Date:  1972-10

6.  Gene deletion and duplication effects on phenotype and gamma globulin levels.

Authors:  N L Rudd; P H Lamarche
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

7.  Partial deletion of the long arm of chromosome 18.

Authors:  A V Mikelsaar; T A Talvik
Journal:  Humangenetik       Date:  1969

8.  [Crying cat syndrome with chromosome mosaicism 46,XY-46,XY,5p-].

Authors:  G Neuhäuser; H Singer; K D Zang
Journal:  Humangenetik       Date:  1968

9.  A deleted B chromosome in a mosaic mother and her cri du chat progeny.

Authors:  J Philip; N J Brandt; B Friis-Hansen; M Mikkelsen; I Tygstrup
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

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
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