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Results: 1-5 |
Results: 5

Authors: Olney, RS Hoyme, HE Roche, F Ferguson, K Hintz, S Madan, A
Citation: Rs. Olney et al., Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): Distinctive features and prenatal detection, AM J MED G, 103(4), 2001, pp. 295-301

Authors: Hoyme, HE
Citation: He. Hoyme, A clinical genetics and dysmorphology approach to growth deficiency, PEDIAT ANN, 29(9), 2000, pp. 549

Authors: Cunniff, C Frias, JL Kaye, C Moeschler, JB Panny, SR Trotter, TL Hanson, JW Williams, J Moore, CA Lloyd-Puryear, M de la Cruz, F Cho, S Desposito, F Hoyme, HE Hall, L
Citation: C. Cunniff et al., Molecular genetic testing in pediatric practice: A subject review, PEDIATRICS, 106(6), 2000, pp. 1494-1497

Authors: Frias, J Levine, LS Oberfield, SE Pang, S Silverstein, J Schwartz, RP Hansen, IL Kaufman, F Varma, SK Oberfield, SE Silverstein, J Levitsky, L Suriano, MJ Poulin, L Cunniff, C Frias, JL Kaye, C Moeschler, JB Panny, SR Trotter, TL de la Cruz, F Hanson, JW Lloyd-Puryear, M Moore, CA Williams, J Hoyme, HE Hall, L
Citation: J. Frias et al., Technical report: Congenital adrenal hyperplasia, PEDIATRICS, 106(6), 2000, pp. 1511-1518

Authors: Witte, MH Erickson, R Bernas, M Andrade, M Reiser, F Conlon, W Hoyme, HE Witte, CL
Citation: Mh. Witte et al., Phenotypic and genotypic heterogeneity in familial Milroy lymphedema, LYMPHOLOGY, 31(4), 1998, pp. 145-155
Risultati: 1-5 |