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Literature DB >> 3570297

A new variant of chromosome 16.

Abstract

A new variant of chromosome 16 with an additional C-band negative segment in the proximal region of the short arm is described. This variant chromosome was found in four cases, two of which were detected prenatally. In three probands the variant chromosome 16 was inherited from a phenotypically normal father.

Mesh：

Year: 1987 PMID： 3570297 DOI： 10.1007/bf00283058

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

12 in total

Review 1. Human chromosomal heteromorphisms: nature and clinical significance.

Authors: R S Verma; H Dosik
Journal: Int Rev Cytol Date: 1980

2. A rare non-heterochromatic 9p+ variant in two amniotic fluid cell cultures.

Authors: N Archidiacono; V Pecile; M Rocchi; L Dalpra; G Nocera; G Simoni
Journal: Prenat Diagn Date: 1984 May-Jun Impact factor: 3.050

Review 3. Aspects of evaluation, significance, and evolution of human C-band heteromorphism.

Authors: B Erdtmann
Journal: Hum Genet Date: 1982 Impact factor: 4.132

4. An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short arm.

Authors: F S Spedicato; A Di Comite; M Tohidast-Akrad
Journal: Clin Genet Date: 1985-08 Impact factor: 4.438

5. Letter: A1 and C9 marker chromosomes in children with combined minor and major malformations.

Authors: J Kunze; G Mau
Journal: Lancet Date: 1975-02-01 Impact factor: 79.321

6. Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss.

Authors: J H Ford; D F Callen; C G Roberts; A B Jahnke
Journal: Hum Genet Date: 1983 Impact factor: 4.132

7. Two unusual G-band variants of the short arm of chromosome 9.

Authors: G R Sutherland; H Eyre
Journal: Clin Genet Date: 1981-05 Impact factor: 4.438

8. Individual variation of centric heterochromatin in man.

Authors: T Brown; F W Robertson; B M Dawson; S J Hanlin; B M Page
Journal: Hum Genet Date: 1980 Impact factor: 4.132

9. C heterochromatin variation in couples with recurrent early abortions.

Authors: A Maes; C Staessen; L Hens; E Vamos; M Kirsch-Volders; M C Lauwers; E Defrise-Gussenhoven; C Susanne
Journal: J Med Genet Date: 1983-10 Impact factor: 6.318

10. Q- and C-band polymorphisms in patients with ovarian or breast carcinoma.

Authors: S Kivi; A V Mikelsaar
Journal: Hum Genet Date: 1980 Impact factor: 4.132

8 in total

Review 1. Chromosome imbalance, normal phenotype, and imprinting.

Authors: L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal: J Med Genet Date: 1990-09 Impact factor: 6.318

2. The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12.

Authors: Rosetta Lecce; Marina Murdolo; Gianfranco Gelli; Katharina Steindl; Livia Coppola; Anna Romano; Elisa Cupelli; Giovanni Neri; Marcella Zollino
Journal: Hum Genet Date: 2005-12-02 Impact factor: 4.132

7. The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)].

Authors: L Hills; E Earle; M Wilson; V Petrovic; L E Voullaire; M Leversha; D M Danks; K H Choo
Journal: Hum Genet Date: 1991-06 Impact factor: 4.132

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