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Literature DB >> 1277572

Y/autosomal translocations.

J Nielsen, K Rasmussen.

Abstract

Mesh：

Year: 1976 PMID： 1277572 DOI： 10.1111/j.1399-0004.1976.tb01621.x

Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438

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Cited

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19 in total

1. Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report.

Authors: Albrecht Röpke; Yvonne Stratis; Dajana Dossow-Scheele; Peter Wieacker; Sabine Kliesch; Frank Tüttelmann
Journal: J Assist Reprod Genet Date: 2013-10-24 Impact factor: 3.412

2. Molecular characterization of a Y;15 translocation segregating in a family.

Authors: T Alitalo; J Tiihonen; P Hakola; A de la Chapelle
Journal: Hum Genet Date: 1988-05 Impact factor: 4.132

3. Amplification of satellite III DNA in an unusually large chromosome 14p+ variant.

Authors: E Earle; S Dale; K H Choo
Journal: Hum Genet Date: 1989-05 Impact factor: 4.132

4. Familial transmission of a translocation Y/14.

Authors: C H Buys; G J Anders; J M Borkent-Ypma; J A Blenkers-Platter; A Y van der Hoek-van der Veen
Journal: Hum Genet Date: 1979 Impact factor: 4.132

5. Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.

Authors: J F Mattei; M G Mattei; J Coignet; F Giraud
Journal: J Med Genet Date: 1978-04 Impact factor: 6.318

Review 6. Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Authors: R M Davis
Journal: J Med Genet Date: 1981-06 Impact factor: 6.318

Y/autosomal translocations.

1. Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report.

2. Molecular characterization of a Y;15 translocation segregating in a family.

3. Amplification of satellite III DNA in an unusually large chromosome 14p+ variant.

4. Familial transmission of a translocation Y/14.

5. Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.

Review 6. Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Review 7. Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

8. Prenatal diagnosis of a de novo Y/22 translocation.

9. AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.

10. Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant.