AAAAAA

   
Results: 1-10 |
Results: 10
Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy14 and monosomy 21
Authors: Lee, C Fowler, DJ Lemyre, E Sandstrom, MM Holmes, LB Morton, CC
Citation: C. Lee et al., Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy14 and monosomy 21, AM J MED G, 100(3), 2001, pp. 246-250
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
Authors: Gong, YQ Slee, RB Fukai, N Rawadi, G Roman-Roman, S Reginato, AM Wang, HW Cundy, T Glorieux, FH Lev, D Zacharin, M Oexle, K Marcelino, J Suwairi, W Heeger, S Sabatakos, G Apte, S Adkins, WN Allgrove, J Arslan-Kirchner, M Batch, JA Beighton, P Black, GCM Boles, RG Boon, LM Borrone, C Brunner, HG Carle, GF Dallapiccola, B De Paepe, A Floege, B Halfhide, ML Hall, B Hennekam, RC Hirose, T Jans, A Juppner, H Kim, CA Keppler-Noreuil, K Kohlschuetter, A LaCombe, D Lambert, M Lemyre, E Letteboer, T Peltonen, L Ramesar, RS Romanengo, M Somer, H Steichen-Gersdorf, E Steinmann, B Sullivan, B Superti-Furga, A Swoboda, W van den Boogaard, MJ Van Hul, V Vikkula, M Votruba, M Zabel, B Garcia, T Baron, R Olsen, BR Warman, ML
Citation: Yq. Gong et al., LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development, CELL, 107(4), 2001, pp. 513-523
Integration of cytogenetic landmarks into the draft sequence of the human genome
Authors: Cheung, VG Nowak, N Jang, W Kirsch, IR Zhao, S Chen, XN Furey, TS Kim, UJ Kuo, WL Olivier, M Conroy, J Kasprzyk, A Massa, H Yonescu, R Sait, S Thoreen, C Snijders, A Lemyre, E Bailey, JA Bruzel, A Burrill, WD Clegg, SM Collins, S Dhami, P Friedman, C Han, CS Herrick, S Lee, J Ligon, AH Lowry, S Morley, M Narasimhan, S Osoegawa, K Peng, Z Plajzer-Frick, I Quade, BJ Scott, D Sirotkin, K Thorpe, AA Gray, JW Hudson, J Pinkel, D Ried, T Rowen, L Shen-Ong, GL Strausberg, RL Birney, E Callen, DF Cheng, JF Cox, DR Doggett, NA Carter, NP Eichler, EE Haussler, D Korenberg, JR Morton, CC Albertson, D Schuler, G de Jong, PJ Trask, BJ
Citation: Vg. Cheung et al., Integration of cytogenetic landmarks into the draft sequence of the human genome, NATURE, 409(6822), 2001, pp. 953-958
Stable non-Robertsonian dicentric chromosomes: four new cases and a review
Authors: Lemyre, E Der Kaloustian, VM Duncan, AMV
Citation: E. Lemyre et al., Stable non-Robertsonian dicentric chromosomes: four new cases and a review, J MED GENET, 38(1), 2001, pp. 76-79
Phenotype of a patient with pure partial trisomy 2p(p23 -> pter)
Authors: Al-Saffar, M Lemyre, E Koenekoop, R Duncan, AMV Der Kaloustian, VM
Citation: M. Al-saffar et al., Phenotype of a patient with pure partial trisomy 2p(p23 -> pter), AM J MED G, 94(5), 2000, pp. 428-432
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p
Authors: Tihy, F Lemyre, E Dallaire, L Lemieux, N
Citation: F. Tihy et al., Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p, AM J MED G, 91(5), 2000, pp. 383-386
Bone dysplasia series - Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update
Authors: Lemyre, E Azouz, EM Teebi, AS Glanc, P Chen, MF
Citation: E. Lemyre et al., Bone dysplasia series - Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update, CAN ASSOC R, 50(3), 1999, pp. 185-197
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype
Authors: Tihy, F Lemyre, E Lemieux, N Dallaire, L
Citation: F. Tihy et al., De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype, AM J MED G, 87(4), 1999, pp. 302-305
Clinical spectrum of infantile free sialic acid storage disease
Authors: Lemyre, E Russo, P Melancon, SB Gagne, R Potier, M Lambert, M
Citation: E. Lemyre et al., Clinical spectrum of infantile free sialic acid storage disease, AM J MED G, 82(5), 1999, pp. 385-391
Prevalence of congenital anomalies at birth among offspring of women at risk for a genetic disorder and with a normal second-trimester ultrasound
Authors: Lemyre, E Infante-Rivard, C Dallaire, L
Citation: E. Lemyre et al., Prevalence of congenital anomalies at birth among offspring of women at risk for a genetic disorder and with a normal second-trimester ultrasound, TERATOLOGY, 60(4), 1999, pp. 240-244
Risultati: 1-10 |