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Items: 1 to 20 of 290

1.

The origin of the extra Y chromosome in males with a 47,XYY karyotype.

Robinson DO, Jacobs PA.

Hum Mol Genet. 1999 Nov;8(12):2205-9.

PMID:
10545600
3.

Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.

Vorsanova SG, Iourov IY, Beresheva AK, Demidova IA, Monakhov VV, Kravets VS, Bartseva OB, Goyko EA, Soloviev IV, Yurov YB.

Tsitol Genet. 2005 Nov-Dec;39(6):30-6.

PMID:
16396318
4.

A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin.

Thomas NS, Collins AR, Hassold TJ, Jacobs PA.

Eur J Hum Genet. 2000 Oct;8(10):805-8.

5.

Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.

Ramírez NJ, Belalcázar HM, Yunis JJ, Quintero LN, Arboleda GH, Arboleda H.

Biomedica. 2007 Mar;27(1):141-8. Epub 2007 May 31.

6.

Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.

Ballesta F, Queralt R, Gómez D, Solsona E, Guitart M, Ezquerra M, Moreno J, Oliva R.

Ann Genet. 1999;42(1):11-5.

PMID:
10214502
7.

Parental origin of autosomal trisomies.

Hassold T, Chiu D, Yamane JA.

Ann Hum Genet. 1984 May;48(Pt 2):129-44.

PMID:
6234852
8.

Non-disjunction of chromosome 13.

Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB.

Hum Mol Genet. 2007 Aug 15;16(16):2004-10. Epub 2007 Jun 21.

PMID:
17584770
9.

Origin and mechanisms of non-disjunction in human autosomal trisomies.

Nicolaidis P, Petersen MB.

Hum Reprod. 1998 Feb;13(2):313-9. Review.

PMID:
9557829
10.

Non-disjunction of chromosome 18.

Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, Hertz JM, Tranebjaerg L, de Lozier-Blanchet C, Nicolaides P, Brøndum-Nielsen K, Morton N, Mikkelsen M.

Hum Mol Genet. 1998 Apr;7(4):661-9.

PMID:
9499419
11.

Parental origin of the extra chromosome in Down's Syndrome.

Mikkelsen M.

J Ment Defic Res. 1982 Sep;26(Pt 3):143-51.

PMID:
6217343
12.

Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.

Park VM, Bravo RR, Shulman LP.

J Med Genet. 1995 Aug;32(8):650-3.

13.

Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females.

Levilliers J, Quack B, Weissenbach J, Petit C.

Proc Natl Acad Sci U S A. 1989 Apr;86(7):2296-300.

14.

Marker chromosomes in parents to children with Down's syndrome.

Annerén G, Wahlström J, Tommerup N.

Clin Genet. 1984 Feb;25(2):140-7.

PMID:
6231142
15.

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.

Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA.

Hum Mol Genet. 2001 Feb 1;10(3):243-50.

PMID:
11159943
16.

Y-chromosome disomy and trisomy in scarabaeid and cerambycid beetles.

Dutrillaux AM, Dutrillaux B.

Cytogenet Genome Res. 2011;132(3):195-202. doi: 10.1159/000321569. Epub 2010 Nov 11.

PMID:
21071925
19.

[On the origin of meiotic errors with special reference to trisomy 21 (author's transl)].

Wagenbichler P.

Wien Klin Wochenschr Suppl. 1976;63:1-23. German.

PMID:
136814
20.

Recombination in the pseudoautosomal region in a 47,XYY male.

Martin RH, Shi Q, Field LL.

Hum Genet. 2001 Aug;109(2):143-5.

PMID:
11511918

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