Literature DB >> 4168631

Deleted chromosome 18 with paternal mosaicism.

E J Day, R Marshall, P A MacDonald, W M Davidson.   

Abstract

Mesh：

Year:  1967        PMID： 4168631     DOI： 10.1016/s0140-6736(67)90418-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  17 in total

1.  Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.

Authors:  Soraya Beiraghi; Swapan K Nath; Matthew Gaines; Desh D Mandhyan; David Hutchings; Uppala Ratnamala; Ken McElreavey; Lucia Bartoloni; Gregory S Antonarakis; Stylianos E Antonarakis; Uppala Radhakrishna
Journal:  Am J Hum Genet       Date:  2007-05-18       Impact factor: 11.025

2.  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

3.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

Review 4.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 5.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 6.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

7.  Preferential breakage of sensitive regions of human chromosomes.

Authors:  B R Reeves; S D Lawler
Journal:  Humangenetik       Date:  1970

8.  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

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

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

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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