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Developmental Biology|June 1, 1988
Polarized site of sperm entrance in the egg of a freshwater bivalve, Unio elongatulusR Focarelli, T Renieri, F Rosati
Tissue Antigens|February 1, 1979
The distribution of HLA antigens and genes in the Greek populationN Renieri, C Stavropoulos, V Lepage
European Journal of Medical Genetics|March 24, 2009
14q12 Microdeletion syndrome and congenital variant of Rett syndromeMaria Antonietta Mencarelli, Tjitske Kleefstra, Eleni Katzaki, et al.
European Journal of Ophthalmology|April 17, 2012
13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twinsSonia De Francesco, Paolo Galluzzi, Alessandra Del Longo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2022
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosisDiego Lopergolo, Gianna Berti, Francesca Mari, et al.
European Journal of Medical Genetics|March 28, 2009
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumbM Pollazzon, S Grosso, F T Papa, et al.
Clinical Genetics|September 13, 2001
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardationA Malandrini, F Mari, S Palmeri, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|July 4, 2006
Blepharophimosis, ptosis, and epicanthus inversus syndrome: clinical and molecular analysis of a caseFrancesca Mari, Daniela Giachino, Lucia Russo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 26, 2007
RSK2 enzymatic assay as a second level diagnostic tool in Coffin-Lowry syndromeVanna Micheli, Sylvia Sestini, Veronica Parri, et al.
Pediatric Nephrology (Berlin, Germany)|March 8, 2011
Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2Vera Uliana, Elena Marcocci, Mafalda Mucciolo, et al.
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