Page DC - Search Results

1

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.

Repping S, van Daalen SK, Korver CM, Brown LG, Marszalek JD, Gianotten J, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Among authors: page dc. Genomics. 2004 Jun;83(6):1046-52. doi: 10.1016/j.ygeno.2003.12.018. Genomics. 2004. PMID: 15177557

2

Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs.

Page DC, Disteche CM, Simpson EM, de la Chapelle A, Andersson M, Alitalo T, Brown LG, Green P, Akots G. Page DC, et al. Genomics. 1990 May;7(1):37-46. doi: 10.1016/0888-7543(90)90516-w. Genomics. 1990. PMID: 1970799

3

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female.

Page DC, Fisher EM, McGillivray B, Brown LG. Page DC, et al. Nature. 1990 Jul 19;346(6281):279-81. doi: 10.1038/346279a0. Nature. 1990. PMID: 1973823

4

Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males.

Page DC, Brown LG, de la Chapelle A. Page DC, et al. Nature. 1987 Jul 30-Aug 5;328(6129):437-40. doi: 10.1038/328437a0. Nature. 1987. PMID: 2886915

5

Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes.

Page DC, Bieker K, Brown LG, Hinton S, Leppert M, Lalouel JM, Lathrop M, Nystrom-Lahti M, de la Chapelle A, White R. Page DC, et al. Genomics. 1987 Nov;1(3):243-56. doi: 10.1016/0888-7543(87)90051-6. Genomics. 1987. PMID: 2895727

6

Characterization of a (Y;4) translocation by DNA hybridization.

Andersson M, Page DC, Brown LG, Elfving K, de la Chapelle A. Andersson M, et al. Among authors: page dc. Hum Genet. 1988 Apr;78(4):377-81. doi: 10.1007/BF00291741. Hum Genet. 1988. PMID: 3360449

7

Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome.

Krauss CM, Turksoy RN, Atkins L, McLaughlin C, Brown LG, Page DC. Krauss CM, et al. Among authors: page dc. N Engl J Med. 1987 Jul 16;317(3):125-31. doi: 10.1056/NEJM198707163170301. N Engl J Med. 1987. PMID: 3600701

8

Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty.

Reijo R, Seligman J, Dinulos MB, Jaffe T, Brown LG, Disteche CM, Page DC. Reijo R, et al. Among authors: page dc. Genomics. 1996 Jul 15;35(2):346-52. doi: 10.1006/geno.1996.0366. Genomics. 1996. PMID: 8661148

9

The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned.

Saxena R, Brown LG, Hawkins T, Alagappan RK, Skaletsky H, Reeve MP, Reijo R, Rozen S, Dinulos MB, Disteche CM, Page DC. Saxena R, et al. Among authors: page dc. Nat Genet. 1996 Nov;14(3):292-9. doi: 10.1038/ng1196-292. Nat Genet. 1996. PMID: 8896558

10

Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction.

Silber SJ, Alagappan R, Brown LG, Page DC. Silber SJ, et al. Among authors: page dc. Hum Reprod. 1998 Dec;13(12):3332-7. doi: 10.1093/humrep/13.12.3332. Hum Reprod. 1998. PMID: 9886509

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