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European Journal of Medical Genetics|November 15, 2011
Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?Periklis Makrythanasis, Stefania Gimelli, Frédérique Béna, et al.Genomics|April 15, 1996
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3M D Lalioti, A Gos, M R Green, et al.Journal of Hazardous Materials|November 2, 2010
Large pore diameter MCM-41 and its application for lead removal from aqueous mediaSalah A Idris, Christine M Davidson, Colm McManamon, et al.AJR. American Journal of Roentgenology|August 24, 2010
Breast MRI after conservation therapy: usual findings in routine follow-up examinationsJie Li, D David Dershaw, Carol H Lee, et al.Biochemical and Biophysical Research Communications|July 30, 1999
The genomic organization and polymorphism analysis of the human Niemann-Pick C1 geneJ A Morris, D Zhang, K G Coleman, et al.Annals of Human Genetics|March 30, 2000
Common HLA alleles, rather than rare mutants, confer susceptibility to coeliac diseaseP M Brett, J Y Yiannakou, M A Morris, et al.Animal Reproduction Science|January 22, 2003
The contribution of the male to ovine embryogenesis in an in vitro embryo production systemLee H A Morris, Adrienne E Randall, W A King, et al.Radiology|November 1, 1996
Overdiagnosis of medullary carcinoma: a mammographic-pathologic correlative studyL Liberman, L R LaTrenta, B Samli, et al.Neurology|February 26, 2004
Phenotypic heterogeneity of dopa-responsive dystonia in monozygotic twinsH Grötzsch, H Schnorf, M A Morris, et al.European Journal of Biochemistry|March 1, 1995
Primary structure of the neuronal clathrin-associated protein auxilin and its expression in bacteriaS Schröder, S A Morris, R Knorr, et al.Pageof 371