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Literature DB >> 5310106

[21 p-maternal in duplicate in a case of trisomy 21].

J de Grouchy.

Abstract

Mesh：

Year: 1970 PMID： 5310106

Source DB: PubMed Journal: Ann Genet ISSN： 0003-3995

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Cited

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10 in total

1. Inversions and other unusual heteromorphisms detected by C-banding.

Authors: M Mayer; J Matsuura; P Jacobs
Journal: Hum Genet Date: 1978-11-24 Impact factor: 4.132

2. Origin of the extra chromosome in trisomy 21.

Authors: J F Mattei; M G Mattei; S Ayme; F Giraud
Journal: Hum Genet Date: 1979-01-19 Impact factor: 4.132

3. Parental origin of the extra chromosome in Down's syndrome.

Authors: R E Magenis; K M Overton; J Chamberlin; T Brady; E Lovrien
Journal: Hum Genet Date: 1977-06-10 Impact factor: 4.132

4. Trisomy 21: association between reduced recombination and nondisjunction.

Authors: S L Sherman; N Takaesu; S B Freeman; M Grantham; C Phillips; R D Blackston; P A Jacobs; A E Cockwell; V Freeman; I Uchida
Journal: Am J Hum Genet Date: 1991-09 Impact factor: 11.025

5. Maternal and paternal origin of extra chromosome in trisomy 21.

Authors: M Mikkelsen; A Hallberg; H Poulsen
Journal: Hum Genet Date: 1976-04-15 Impact factor: 4.132

6. On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphisms.

Authors: U Langenbeck; I Hansmann; B Hinney; V Hönig
Journal: Hum Genet Date: 1976-07-27 Impact factor: 4.132

[21 p-maternal in duplicate in a case of trisomy 21].

1. Inversions and other unusual heteromorphisms detected by C-banding.

2. Origin of the extra chromosome in trisomy 21.

3. Parental origin of the extra chromosome in Down's syndrome.

4. Trisomy 21: association between reduced recombination and nondisjunction.

5. Maternal and paternal origin of extra chromosome in trisomy 21.

6. On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphisms.

7. On the origin of chromosome anomaly.

8. Trisomy 21: origin of non-disjunction.

9. Origin of the additional chromosome in Down's syndrome: a study of 20 families.

10. Clustering of chromosomal aneuploidy and tracing of nondisjunction in man.