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Literature DB >> 10830017

Partial trisomy 18q.

M Elbistan¹, S Kucukoduk, N Kara.

Abstract

Mesh：

Year: 1996 PMID： 10830017 DOI： 10.1007/bf02751537

Source DB: PubMed Journal: Indian J Pediatr ISSN： 0019-5456 Impact factor: 1.967

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13 in total

1. Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors: P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal: Exp Cell Res Date: 1960-09 Impact factor: 3.905

Review 2. Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18.

Authors: G N Wilson; K B Heller; R D Elterman; N R Schneider
Journal: Am J Med Genet Date: 1990-08

Review 3. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).

Authors: T Asano; T Ikeuchi; T Shinohara; H Enokido; K Hashimoto
Journal: Jinrui Idengaku Zasshi Date: 1991-09

4. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).

Authors: E Pluchon; Y Giovangrandi; F Labbe; M J Le Bris; M Collet; J P Brettes; D Riviere; M R Riviere
Journal: Prenat Diagn Date: 1993-10 Impact factor: 3.050

5. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.

Authors: D J Wolff; M F Schwartz; M M Cohen; S Schwartz
Journal: Am J Med Genet Date: 1993-06-15

6. Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Authors: R L Neu; C C Ortega; G A Barg; W Pinto; L I Gardner; W M Howell; T E Denton
Journal: J Med Genet Date: 1976-12 Impact factor: 6.318

Partial trisomy 18q.

1. Chromosome preparations of leukocytes cultured from human peripheral blood.

Review 2. Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18.

Review 3. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).

4. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).

5. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.

6. Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

7. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.

8. Partial trisomy 18q in a newborn with typical 18 trisomy phenotype.

Review 9. Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

10. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].