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American Journal of Medical Genetics|February 1, 1991
X-linked mental retardation with marfanoid habitus: first report of four Italian patientsF Lalatta, E Livini, A Selicorni, et al.American Journal of Medical Genetics. Part A|April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehogLivia Garavelli, C Zanacca, G Caselli, et al.Neurology|April 1, 1997
The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsyA Battaglia, F Gurrieri, E Bertini, et al.Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.American Journal of Medical Genetics|October 2, 2001
Rearrangements of chromosome 15 in epilepsyL Torrisi, E Sangiorgi, L Russo, et al.American Journal of Medical Genetics|July 1, 1984
Some questions on the significance of chromosome alterations in leukemias and lymphomas: a reviewG NeriGiornale Italiano Di Medicina Del Lavoro Ed Ergonomia|March 19, 2004
[Influence of genetic polymorphism of CYP1A1 and GSTM1 on the levels of urinary 1-hydroxypyrene]G NeriAmerican Journal of Medical Genetics|June 1, 1984
A possible explanation for the low incidence of gonosomal aneuploidy among the offspring of triplo-X individualsG NeriAmerican Journal of Medical Genetics|May 17, 1996
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regionsG Sebastio, L Perone, V Guzzetta, et al.American Journal of Medical Genetics|April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25F Gurrieri, P Prinos, D Tackels, et al.Pageof 49