Literature DB >> 14180960

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

J DE GROUCHY, P ROYER, C SALMON, M LAMY.   

Abstract

Entities:  

Keywords:  BLOOD GROUPS; CHROMOSOME ABNORMALITIES; DERMATOGLYPHICS; DIAGNOSIS; INFANT

Mesh：

Substances：

Year:  1964        PMID： 14180960

Source DB:  PubMed          Journal:  Pathol Biol


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  45 in total

1.  Adult-onset seizure disorder in the 18q deletion syndrome.

Authors:  N Adab; A J Larner
Journal:  J Neurol       Date:  2006-03-20       Impact factor: 4.849

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

3.  Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.

Authors:  M G Wilson; M S Lin
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

4.  18Q - syndrome resulting from a tdic(14p; 18q).

Authors:  J C Lambert; M Ferrari; C Bergondi; A Galliana; N Ayraud
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

Review 5.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 6.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 7.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

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

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

9.  18q-syndrome and extraskeletal Ewing's sarcoma.

Authors:  M Machin Valtueña; J M Garcia-Sagredo; A Muñoz Villa; C Lozano Giménez; J M Aparicio Meix
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

10.  The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Authors:  G A Silverman; S S Schneider; H F Massa; A Flint; M Lalande; J C Leonard; J Overhauser; G van den Engh; B J Trask
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025
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