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Results: 1-10 |
Results: 10
Molecular analysis of genes on Xp controlling turner syndrome and premature ovarian failure (POF)
Authors: Zinn, AR Ross, JL
Citation: Ar. Zinn et Jl. Ross, Molecular analysis of genes on Xp controlling turner syndrome and premature ovarian failure (POF), SEMIN REP M, 19(2), 2001, pp. 141-146
The X chromosome and the ovary
Authors: Zinn, AR
Citation: Ar. Zinn, The X chromosome and the ovary, J SOC GYN I, 8(1), 2001, pp. S34-S36
A fork in the road to fertility
Authors: Prueitt, RL Zinn, AR
Citation: Rl. Prueitt et Ar. Zinn, A fork in the road to fertility, NAT GENET, 27(2), 2001, pp. 132-134
A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from hismother and neurofibromatosis type 1 from his father
Authors: Wei, FL Cheng, S Badie, N Elder, F Scott, C Nicholson, L Ross, JL Zinn, AR
Citation: Fl. Wei et al., A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from hismother and neurofibromatosis type 1 from his father, AM J MED G, 102(4), 2001, pp. 353-358
Profound obesity associated with a balanced translocation that disrupts the SIM1 gene
Authors: Holder, JL Butte, NF Zinn, AR
Citation: Jl. Holder et al., Profound obesity associated with a balanced translocation that disrupts the SIM1 gene, HUM MOL GEN, 9(1), 2000, pp. 101-108
Assignment of Microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization
Authors: Inoue, N Wei, F Seldin, MF Zinn, AR Watson, ML
Citation: N. Inoue et al., Assignment of Microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization, CYTOG C GEN, 90(1-2), 2000, pp. 123-125
Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene
Authors: Prueitt, RL Ross, JL Zinn, AR
Citation: Rl. Prueitt et al., Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene, CYTOG C GEN, 89(1-2), 2000, pp. 44-50
The Burner syndrome-associated neurocognitive phenotype maps to distal Xp
Authors: Ross, JL Roeltgen, D Kushner, H Wei, FL Zinn, AR
Citation: Jl. Ross et al., The Burner syndrome-associated neurocognitive phenotype maps to distal Xp, AM J HU GEN, 67(3), 2000, pp. 672-681
New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis
Authors: Inoue, N Hess, KD Moreadith, RW Richardson, LL Handel, MA Watson, ML Zinn, AR
Citation: N. Inoue et al., New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis, HUM MOL GEN, 8(7), 1999, pp. 1201-1207
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1
Authors: Zinn, AR Tonk, VS Chen, Z Flejter, WL Gardner, HA Guerra, R Kushner, H Schwartz, S Sybert, VP Van Dyke, DL Ross, JL
Citation: Ar. Zinn et al., Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1, AM J HU GEN, 63(6), 1998, pp. 1757-1766
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