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Results: 1-9 |
Results: 9
A novel X chromosome-linked genetic cause of recurrent spontaneous abortion
Authors: Lanasa, MC Hogge, WA Kubik, CJ Ness, RB Harger, J Nagel, T Prosen, T Markovic, N Hoffman, EP
Citation: Mc. Lanasa et al., A novel X chromosome-linked genetic cause of recurrent spontaneous abortion, AM J OBST G, 185(3), 2001, pp. 563-568
A single physician's experience with four thousand six hundred genetic amniocenteses - Discussion
Authors: Jones, S Hogge, WA Christmas, J Johnson, J Horger, EO
Citation: S. Jones et al., A single physician's experience with four thousand six hundred genetic amniocenteses - Discussion, AM J OBST G, 185(2), 2001, pp. 287-288
Maternal serum screening for fetal trisomy 18: Benefits of patient-specific risk protocol
Authors: Hogge, WA Fraer, L Melegari, T
Citation: Wa. Hogge et al., Maternal serum screening for fetal trisomy 18: Benefits of patient-specific risk protocol, AM J OBST G, 185(2), 2001, pp. 289-291
X chromosome defects as an etiology of recurrent spontaneous abortion
Authors: Lanasa, MC Hogge, WA
Citation: Mc. Lanasa et Wa. Hogge, X chromosome defects as an etiology of recurrent spontaneous abortion, SEMIN REP M, 18(1), 2000, pp. 97-103
Second-trimester levels of maternal serum human chorionic gonadotropin andinhibin A as predictors of preeclampsia in the third trimester of pregnancy
Authors: Lambert-Messerlian, GM Silver, HM Petraglia, F Luisi, S Pezzani, I Maybruck, WM Hogge, WA Hanley-Yanez, K Roberts, JM Neveux, LM Canick, JA
Citation: Gm. Lambert-messerlian et al., Second-trimester levels of maternal serum human chorionic gonadotropin andinhibin A as predictors of preeclampsia in the third trimester of pregnancy, J SOC GYN I, 7(3), 2000, pp. 170-174
Multiple marker screening and ultrasound can identify triploid fetuses in early gestation
Authors: Lazebnik, N Surti, U Smith, E Fraer, L Hogge, WA
Citation: N. Lazebnik et al., Multiple marker screening and ultrasound can identify triploid fetuses in early gestation, PRENAT N M, 4(2), 1999, pp. 113-119
Insights into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney disease
Authors: Lazebnik, N Bellinger, MF Ferguson, JE Hogge, JS Hogge, WA
Citation: N. Lazebnik et al., Insights into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney disease, PRENAT DIAG, 19(5), 1999, pp. 418-423
Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion
Authors: Lanasa, MC Hogge, WA Kubik, C Blancato, J Hoffman, EP
Citation: Mc. Lanasa et al., Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion, AM J HU GEN, 65(1), 1999, pp. 252-254
The X chromosome and recurrent spontaneous abortion: The significance of transmanifesting carriers
Authors: Lanasa, MC Hogge, WA Hoffman, EP
Citation: Mc. Lanasa et al., The X chromosome and recurrent spontaneous abortion: The significance of transmanifesting carriers, AM J HU GEN, 64(4), 1999, pp. 934-938
Risultati: 1-9 |