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Literature DB >> 1002157

Trisomy 9 associated with an enlarged 9qh segment in a liveborn.

Abstract

This report describes the third case of a complete trisomy 9 in a liveborn infant. A tentative explanation for the origin of a "very large" h-segment which was not present in either parent of the proposita is put forward.

Entities: Disease Species

Mesh：

Year: 1976 PMID： 1002157 DOI： 10.1007/bf00295299

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

7 in total

1. Prenatal diagnosis of trisomy 9.

Authors: U Francke; K Benirschke; O W Jones
Journal: Humangenetik Date: 1975-09-23

2. Partial and complete trisomy 9: delineation of a trisomy 9 syndrome.

Authors: G R Sutherland; R F Carter; L L Morris
Journal: Hum Genet Date: 1976-05-19 Impact factor: 4.132

3. Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.

Authors: J Nielsen; U Friedrich; A B Hreidarsson; E Zeuthen
Journal: Humangenetik Date: 1974

4. A simple technique for demonstrating centromeric heterochromatin.

Authors: A T Sumner
Journal: Exp Cell Res Date: 1972-11 Impact factor: 3.905

5. A rapid banding technique for human chromosomes.

Authors: M Seabright
Journal: Lancet Date: 1971-10-30 Impact factor: 79.321

6. A case of trisomy 9.

Authors: M Feingold; L Atkins
Journal: J Med Genet Date: 1973-06 Impact factor: 6.318

7. Banding analysis of abnormal karyotypes in spontaneous abortion.

Authors: T Kajii; K Oama; N Niikawa; A Ferrier; S Avirachan
Journal: Am J Hum Genet Date: 1973-09 Impact factor: 11.025

7 in total

13 in total

1. 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

2. The evolution of restricted recombination and the accumulation of repeated DNA sequences.

Authors: B Charlesworth; C H Langley; W Stephan
Journal: Genetics Date: 1986-04 Impact factor: 4.562

Review 3. Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.

Authors: E M Kuhn; G E Sarto; B J Bates; E Therman
Journal: Hum Genet Date: 1987-11 Impact factor: 4.132

4. Delineation of trisomy 9 syndrome.

Authors: D R Romain; J Sullivan
Journal: J Med Genet Date: 1983-04 Impact factor: 6.318

5. Complete trisomy 9 in two liveborn infants.

Authors: S Mantagos; J W McReynolds; M R Seashore; W R Breg
Journal: J Med Genet Date: 1981-10 Impact factor: 6.318

6. Delineation of trisomy 9.

Authors: G S Frohlich
Journal: J Med Genet Date: 1982-08 Impact factor: 6.318

7. Report of a new case and clinical delineation of mosaic trisomy 9 syndrome.

Authors: J M Sánchez; N Fijtman; A M Migliorini
Journal: J Med Genet Date: 1982-10 Impact factor: 6.318

8. Trisomy 9 mosaicism with punctate mineralization in developing cartilages.

Authors: A Akatsuka; O Nishiya; T Kitagawa; A Kageyama; I Inana; Y Nakagome
Journal: Eur J Pediatr Date: 1979-08 Impact factor: 3.183

Review 9. Pericentric inversions. Problems and significance for clinical genetics.

Authors: P Kaiser
Journal: Hum Genet Date: 1984 Impact factor: 4.132

10. On the mode of evolution of alpha satellite DNA in human populations.

Authors: B Marçais; J P Charlieu; B Allain; E Brun; M Bellis; G Roizès
Journal: J Mol Evol Date: 1991-07 Impact factor: 2.395