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Results: 1-7 |
Results: 7
A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion
Authors: Stratakis, CA Turner, ML Lafferty, A Toro, JR Hill, S Meck, JM Blancato, J
Citation: Ca. Stratakis et al., A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion, J MED GENET, 38(5), 2001, pp. 338-343
Trisomy 7p resulting from 7p15;9p24 translocation: Report of a new case and review of associated medical complications
Authors: Kozma, C Haddad, BR Meck, JM
Citation: C. Kozma et al., Trisomy 7p resulting from 7p15;9p24 translocation: Report of a new case and review of associated medical complications, AM J MED G, 91(4), 2000, pp. 286-290
Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)
Authors: Stratakis, CA Lafferty, A Taymans, SE Gafni, RI Meck, JM Blancato, J
Citation: Ca. Stratakis et al., Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503), J CLIN END, 85(9), 2000, pp. 3396-3401
Cytogenetic analysis using telemedicine consultation: An improved means ofproviding expert cross-coverage
Authors: Meck, JM Munshi, G Plempel, J Amato, S Macedonia, C
Citation: Jm. Meck et al., Cytogenetic analysis using telemedicine consultation: An improved means ofproviding expert cross-coverage, GENET MED, 1(7), 1999, pp. 328-331
Detection of Mosaicism in amniotic fluid cultures: A CYTO2000 collaborative study
Authors: Ing, PS Van Dyke, DL Caudill, SP Reidy, JA Bice, G Bieber, FR Buchanan, PD Carroll, AJ Cheung, SW DeWald, G Donahue, RP Gardner, HA Higgins, J Hsu, LYF Jamehdor, M Keitges, EA Laundon, CH Luthardt, FW Mascarello, J May, KM Meck, JM Morton, C Patil, S Peakman, D Pettenati, MJ Rao, N Sanger, WG Saxe, DF Schwartz, S Sekhon, GS Vance, GH Wyandt, HE Yu, CW Zenger-Hain, J Chen, ATL
Citation: Ps. Ing et al., Detection of Mosaicism in amniotic fluid cultures: A CYTO2000 collaborative study, GENET MED, 1(3), 1999, pp. 94-97
Risk of abnormal triple screen for Down syndrome is significantly higher in patients with female fetuses
Authors: Spong, CY Ghidini, A Stanley-Christian, H Meck, JM Seydel, FD Pezzullo, JC
Citation: Cy. Spong et al., Risk of abnormal triple screen for Down syndrome is significantly higher in patients with female fetuses, PRENAT DIAG, 19(4), 1999, pp. 337-339
Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia
Authors: Kozma, C Chong, SS Meck, JM
Citation: C. Kozma et al., Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia, AM J MED G, 86(4), 1999, pp. 316-320
Risultati: 1-7 |