178 related articles for article (PubMed ID: 1674717)
21. The parental origin of 47,XXY males.
Harvey J; Jacobs PA; Hassold T; Pettay D
Birth Defects Orig Artic Ser; 1990; 26(4):289-96. PubMed ID: 2090327
[TBL] [Abstract][Full Text] [Related]
22. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group.
Antonarakis SE
N Engl J Med; 1991 Mar; 324(13):872-6. PubMed ID: 1825697
[TBL] [Abstract][Full Text] [Related]
23. Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.
Jacobs PA; Hassold TJ; Whittington E; Butler G; Collyer S; Keston M; Lee M
Ann Hum Genet; 1988 May; 52(2):93-109. PubMed ID: 2907853
[TBL] [Abstract][Full Text] [Related]
24. Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping.
Meijer H; Hamers GJ; Jongbloed RJ; Vaes-Peeters GP; van der Hulst RR; Geraedts JP
Hum Genet; 1989 Oct; 83(3):280-6. PubMed ID: 2571564
[TBL] [Abstract][Full Text] [Related]
25. Parental age and the origin of extra chromosome 21 in Down syndrome.
Jyothy A; Kumar KS; Mallikarjuna GN; Babu Rao V; Uma Devi B; Sujatha M; Reddy PP
J Hum Genet; 2001; 46(6):347-50. PubMed ID: 11393539
[TBL] [Abstract][Full Text] [Related]
26. Origin of the extra chromosome in trisomy 21.
Mattei JF; Mattei MG; Ayme S; Giraud F
Hum Genet; 1979 Jan; 46(1):107-10. PubMed ID: 155033
[TBL] [Abstract][Full Text] [Related]
27. Clustering of chromosomal aneuploidy and tracing of nondisjunction in man.
Hansmann I
Environ Health Perspect; 1979 Aug; 31():23-5. PubMed ID: 159172
[TBL] [Abstract][Full Text] [Related]
28. Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization.
Müller U; Schneider NR; Marks JF; Kupke KG; Wilson GN
Hum Genet; 1990 Feb; 84(3):289-92. PubMed ID: 2303249
[TBL] [Abstract][Full Text] [Related]
29. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes.
Kovaleva NV; Mutton DE
Am J Med Genet A; 2005 Apr; 134A(1):24-32. PubMed ID: 15704133
[TBL] [Abstract][Full Text] [Related]
30. 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. PubMed ID: 10214502
[TBL] [Abstract][Full Text] [Related]
31. Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.
Howard CM; Davies GE; Farrer MJ; Cullen LM; Coleman MM; Williamson R; Wyse RK; Palmer R; Kessling AM
Am J Hum Genet; 1993 Aug; 53(2):462-71. PubMed ID: 8101041
[TBL] [Abstract][Full Text] [Related]
32. Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype.
Rives N; Joly G; Machy A; Siméon N; Leclerc P; Macé B
Mol Hum Reprod; 2000 Feb; 6(2):107-12. PubMed ID: 10655452
[TBL] [Abstract][Full Text] [Related]
33. Sperm aneuploidy in fathers of children with paternally and maternally inherited Klinefelter syndrome.
Eskenazi B; Wyrobek AJ; Kidd SA; Lowe X; Moore D; Weisiger K; Aylstock M
Hum Reprod; 2002 Mar; 17(3):576-83. PubMed ID: 11870106
[TBL] [Abstract][Full Text] [Related]
34. Crossing over and chromosome 21 nondisjunction: a study of 60 families.
Perroni L; Dagna Bricarelli F; Grasso M; Pierluigi M; Baldi M; Pedemonte C; Strigini P
Am J Med Genet Suppl; 1990; 7():141-7. PubMed ID: 1981474
[TBL] [Abstract][Full Text] [Related]
35. Down-Klinefelter syndrome (48,XXY,+21) in a neonate associated with congenital heart disease.
Rodrigues MA; Morgade LF; Dias LFA; Moreira RV; Maia PD; Sales AFH; Ribeiro PD
Genet Mol Res; 2017 Sep; 16(3):. PubMed ID: 28973759
[TBL] [Abstract][Full Text] [Related]
36. [The parental origin of the extra chromosome 21 in Down's syndrome].
Hamers AJ; Heijnen GC; Jongbloet PH
Tijdschr Kindergeneeskd; 1983 Oct; 51(5):157-62. PubMed ID: 6230758
[TBL] [Abstract][Full Text] [Related]
37. Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome.
Galt J; Boyd E; Connor JM; Ferguson-Smith MA
Hum Genet; 1989 Jan; 81(2):113-9. PubMed ID: 2563248
[TBL] [Abstract][Full Text] [Related]
38. Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis.
Estop AM; Munné S; Cieply KM; Vandermark KK; Lamb AN; Fisch H
Hum Reprod; 1998 Jan; 13(1):124-7. PubMed ID: 9512242
[TBL] [Abstract][Full Text] [Related]
39. 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. PubMed ID: 17546231
[TBL] [Abstract][Full Text] [Related]
40. Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridization.
Blanco J; Egozcue J; Vidal F
Hum Reprod; 2001 May; 16(5):887-92. PubMed ID: 11331634
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]