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Results: 1-4 |
Results: 4
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (vol 9, pg 367, 2000)
Authors: Bejjani, BA Stockton, DW Lewis, RA Tomey, KF Dueker, DK Jabak, M Astle, WF Lupski, JR
Citation: Ba. Bejjani et al., Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (vol 9, pg 367, 2000), HUM MOL GEN, 9(7), 2000, pp. 1141-1141
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus
Authors: Bejjani, BA Stockton, DW Lewis, RA Tomey, KF Dueker, DK Jabak, M Astle, WF Lupski, JR
Citation: Ba. Bejjani et al., Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus, HUM MOL GEN, 9(3), 2000, pp. 367-374
Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): Significance for Ullrich-Turner syndrome screening in the cytogenetics laboratory
Authors: Atkins, KE Gregg, A Spikes, AS Bacino, CA Bejjani, BA Kirkland, J Shaffer, LG
Citation: Ke. Atkins et al., Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): Significance for Ullrich-Turner syndrome screening in the cytogenetics laboratory, AM J MED G, 91(5), 2000, pp. 377-382
Pure trisomy 10p involving an isochromosome 10p
Authors: Berend, SA Shaffer, LG Bejjani, BA
Citation: Sa. Berend et al., Pure trisomy 10p involving an isochromosome 10p, CLIN GENET, 55(5), 1999, pp. 367-371
Risultati: 1-4 |