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Items: 1 to 20 of 90

1.

Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21.

Ghosh D, Sinha S, Chatterjee A, Nandagopal K.

Indian J Hum Genet. 2012 May;18(2):204-16. doi: 10.4103/0971-6866.100769.

2.

A study of GluK1 kainate receptor polymorphisms in Down syndrome reveals allelic non-disjunction at 1173(C/T).

Ghosh D, Sinha S, Chatterjee A, Nandagopal K.

Dis Markers. 2009;27(2):45-54. doi: 10.3233/DMA-2009-0647.

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.

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.

5.

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
6.

[Polymorphisms of seven short tandem repeat loci: D1S2142, D1S3733, D2S1774, D3S2459, D21S1409, D21S1437 and D21S2055 of Chinese Han population in Chengdu].

Wu J, Li YB, Hou YP, Zhang J, Yan J, Liao M, Lin JD, He Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):230-3. Chinese.

PMID:
16604506
7.

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
8.

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

Savage AR, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torfs C, Mikkelsen M, Hassold TJ, Sherman SL.

Hum Mol Genet. 1998 Aug;7(8):1221-7.

PMID:
9668162
9.

A probability model for the meiosis I non-disjunction fraction in numerical chromosomal anomalies.

Franco GC, Lucio PS, Parra FC, Pena SD.

Stat Med. 2003 Jun 30;22(12):2015-24.

PMID:
12802819
10.
11.

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.

Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, Sherman SL.

Nat Genet. 1996 Dec;14(4):400-5.

PMID:
8944019
12.

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
13.

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
14.

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
15.

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
16.

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome.

Davies KE, Harper K, Bonthron D, Krumlauf R, Polkey A, Pembrey ME, Williamson R.

Hum Genet. 1984;66(1):54-6.

PMID:
6230306
17.

Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX.

Reish O, Berryman T, Cunningham TR, Sher C, Oetting WS.

Chromosome Res. 2004;12(2):125-32.

PMID:
15053482
18.

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL.

Hum Mol Genet. 1997 Sep;6(9):1391-9.

PMID:
9285774
19.

[Genetic polymorphisms of short tandem repeat loci D3S1358, D13S317, D5S818 from Nongqu Mongolia].

Liu SP, Su XL, Bi LF, Li CP, Qiu L, Wang FQ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):297-8. Chinese.

PMID:
15192844
20.

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.

Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, Brondum-Nielsen K, Christian SL, Ledbetter DH, Schinzel AA, Horsthemke B, Schuffenhauer S, Michaelis RC, Langlois S, Hassold TJ.

Hum Mol Genet. 1998 Jun;7(6):1011-9.

PMID:
9580665

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