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Clinical Genetics|September 3, 2010
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricleAlessandro De Luca, A Sarkozy, R Ferese, et al.Human Genetics|February 1, 1996
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cellsA Massari, G Novelli, A Colosimo, et al.European Journal of Medical Genetics|November 11, 2021
Congenital heart defects in the recurrent 2q13 deletion syndromeM C Digilio, M L Dentici, S Loddo, et al.Clinical Genetics|December 6, 2012
Syndromic non-compaction of the left ventricle: associated chromosomal anomaliesM C Digilio, L Bernardini, M G Gagliardi, et al.Journal of Medical Genetics|December 7, 2007
Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplificationA De Luca, I Bottillo, M C Dasdia, et al.Neurology|September 17, 1999
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13S Servidei, F Capon, A Spinazzola, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystoniaF Brancati, E M Valente, M Castori, et al.Human Molecular Genetics|July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity geneA Pizzuti, F Amati, G Calabrese, et al.Neurology|September 10, 2009
Effect of a CYP2D6 polymorphism on the efficacy of donepezil in patients with Alzheimer diseaseAlberto Pilotto, M Franceschi, G D'Onofrio, et al.Neuropediatrics|January 4, 2005
Fetal cells in maternal blood: a six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: a multicenter studyE Falcidia, E Parano, A Grillo, et al.Pageof 34