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Literature DB >> 885544

Pitfalls in the use of chromosome variants for paternity dispute cases.

Y Nakagome, T Kitagawa, K Iinuma, E Matsunaga, T Shinoda.

Abstract

A huge 'satellite' (22s+) was observed in a mentally retarded and malformed girl. It consisted of constitutive heterochromatin based on the C-band technique (CBG). In neither of the parents was the variant observed. Genetic marker studies revealed that the father was, indeed, the father of the proposita (probability, 99.8%). It is emphasized that caution must be taken in the use of chromosome variants for paternity dispute cases.

Entities: Disease Gene Species

Mesh：

Substances：
Heterochromatin

Year: 1977 PMID： 885544 DOI： 10.1007/bf00393606

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

12 in total

1. Enlarged satellites as a familial chromosome marker.

Authors: H L COOPER; K HIRSCHHORN
Journal: Am J Hum Genet Date: 1962-06 Impact factor: 11.025

2. Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual.

Authors: H Müller; H P Klinger; M Glasser
Journal: Cytogenet Cell Genet Date: 1975

3. Human Q and C chromosomal variations: distribution and incidence.

Authors: W H McKenzie; H A Lubs
Journal: Cytogenet Cell Genet Date: 1975

4. HL-A antigens and heteromorphic fluorescence characters of chromosomes in prenatal paternity investigation.

Authors: J Jonasson; J Lindsten; R Lundborg; F Kissmeyer-Nielsen; L U Lamm; G B Petersen; A J Therkelsen
Journal: Nature Date: 1972-04-07 Impact factor: 49.962

5. Polymorphism of human C-band heterochromatin. I. Frequency of variants.

Authors: A P Craig-Holmes; F B Moore; M W Shaw
Journal: Am J Hum Genet Date: 1973-03 Impact factor: 11.025

6. Localization of heterochromatin in human chromosomes.

Authors: F E Arrighi; T C Hsu
Journal: Cytogenetics Date: 1971

7. Segregation of genetic markers in families with chromosome polymorphisms and structural rearrangements involving chromosome 1.

Authors: P J Cook; E B Robson; K E Buckton; P A Jacobs; P E Polani
Journal: Ann Hum Genet Date: 1974-01 Impact factor: 1.670

8. [A case of XX-XY chimerism with normal male phenotype (author's transl)].

Authors: K Sperling; R Kaden; K E Gillert; W Weise
Journal: Humangenetik Date: 1974

9. Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.

Authors: A P Craig-Holmes; F B Moore; M W Shaw
Journal: Am J Hum Genet Date: 1975-03 Impact factor: 11.025

10. C- and Q-band polymorphisms in the chromosomes of three human populations.

Authors: K E Buckton; M L O'Riordan; P A Jacobs; J A Robinson; R Hill; H J Evans
Journal: Ann Hum Genet Date: 1976-07 Impact factor: 1.670

6 in total

1. LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants.

Authors: Y Nakagome; S Oka; E Matsunaga
Journal: Hum Genet Date: 1977-10-14 Impact factor: 4.132

2. Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement.

Authors: P Balícek; J Zizka; H Skalská
Journal: Hum Genet Date: 1978-06-27 Impact factor: 4.132