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Clinical Genetics|October 19, 2010
Aberrant PKD2 splicing due to a presumed novel missense mutation in autosomal-dominant polycystic kidney diseaseY-C Tan, J Blumenfeld, A Michaeel, et al.
Clinical Genetics|March 20, 2014
Autosomal dominant polycystic kidney disease caused by somatic and germline mosaicismA Y Tan, J Blumenfeld, A Michaeel, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|December 20, 1999
A novel, non-nested reverse-transcriptase polymerase chain reaction (RT-PCR) test for the detection of the t(15;17) translocation: a comparative study of RT-PCR cytogenetics, and fluorescence In situ hybridizationH Rennert, T Golde, R B Wilson, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|October 24, 1998
Novel bcl-2 breakpoints in patients with follicular lymphomaY L Wang, K Addya, R H Edwards, et al.
American Journal of Medical Genetics|July 16, 1999
Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophyK L Chen, Y L Wang, H Rennert, et al.
The Journal of Steroid Biochemistry and Molecular Biology|January 6, 2012
Oncogene-transformed granulosa cells as a model system for the study of steroidogenic processesA Amsterdam, I Hanukoglu, B S Suh, et al.
Neurology|September 26, 1997
Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT geneP M Bingham, N Shen, H Rennert, et al.
Genomics|November 15, 1994
The structure of the human sterol carrier protein X/sterol carrier protein 2 gene (SCP2)T Ohba, H Rennert, S M Pfeifer, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Sterol carrier protein 2: a role in steroid hormone synthesis?S M Pfeifer, E E Furth, T Ohba, et al.
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