Literature DB >> 5507053

Familial occurrence of 18q.

I Subrt, J Pokorný.   

Abstract

Mesh：

Year:  1970        PMID： 5507053     DOI： 10.1007/bf00295518

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  6 in total

1.  [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors:  J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal:  Pathol Biol       Date:  1964-05

2.  Deleted chromosome 18 with paternal mosaicism.

Authors:  E J Day; R Marshall; P A MacDonald; W M Davidson
Journal:  Lancet       Date:  1967-12-16       Impact factor: 79.321

3.  Partial E-18 long-arm deletion.

Authors:  W E Nance; S H Higdon; B Chown; E Engel
Journal:  Lancet       Date:  1968-02-10       Impact factor: 79.321

4.  [A study of IgA, G and M in five cases of partial deletion of chromosome 18].

Authors:  J de Grouchy; F Danon
Journal:  Ann Genet       Date:  1969-06

5.  Familial 18 q- syndrome.

Authors:  E M Law; J G Masterson
Journal:  Ann Genet       Date:  1969-12

6.  IgA deficiency associated with partial deletion of chromosome 18.

Authors:  M Feingold; R S Schwartz; L Atkins; R Anderson; C S Bartsocas; D L Page; J W Littlefield
Journal:  Am J Dis Child       Date:  1969-02
  6 in total
  12 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.  Molecular characterization of patients with 18q23 deletions.

Authors:  G Strathdee; R Sutherland; J J Jonsson; R Sataloff; M Kohonen-Corish; D Grady; J Overhauser
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 3.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 4.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 5.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

6.  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 7.  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

Review 8.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

9.  Interstitial deletions are not the main mechanism leading to 18q deletions.

Authors:  G Strathdee; W Harrison; H C Riethman; S A Goodart; J Overhauser
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

10.  High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).

Authors:  Patricia L Heard; Erika M Carter; Analisa C Crandall; Courtney Sebold; Daniel E Hale; Jannine D Cody
Journal:  Am J Med Genet A       Date:  2009-07       Impact factor: 2.802
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