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Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
Zinn AR, Tonk VS, Chen Z, Flejter WL, Gardner HA, Guerra R, Kushner H, Schwartz S, Sybert VP, Van Dyke DL, Ross JL. Zinn AR, et al. Among authors: flejter wl. Am J Hum Genet. 1998 Dec;63(6):1757-66. doi: 10.1086/302152. Am J Hum Genet. 1998. PMID: 9837829 Free PMC article.
Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13.
Flejter WL, McDaniel LD, Askari M, Friedberg EC, Schultz RA. Flejter WL, et al. Genes Chromosomes Cancer. 1992 Nov;5(4):335-42. doi: 10.1002/gcc.2870050409. Genes Chromosomes Cancer. 1992. PMID: 1283322
We have recently reported the identification of a single rearranged human chromosome, designated Tneo, which corrects the UV sensitivity and excision repair defect of cells of xeroderma pigmentosum genetic complementation group D (XP-D) in culture (Flejter WL et al. …
We have recently reported the identification of a single rearranged human chromosome, designated Tneo, which corrects the UV sensitivity and …
A practical metaphase marker of the inactive X chromosome.
Van Dyke DL, Flejter WL, Worsham MJ, Roberson JR, Higgins JV, Herr HM, Knuutila S, Wang N, Babu VR, Weiss L. Van Dyke DL, et al. Among authors: flejter wl. Am J Hum Genet. 1986 Jul;39(1):88-95. Am J Hum Genet. 1986. PMID: 3463206 Free PMC article.
Familial ring (19) chromosome mosaicism: case report and review.
Flejter WL, Finlinson D, Root S, Nguyen W, Brothman AR, Viskochil D. Flejter WL, et al. Am J Med Genet. 1996 Dec 18;66(3):276-80. doi: 10.1002/(SICI)1096-8628(19961218)66:3<276::AID-AJMG8>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8985487 Review.
34 results