Showing results (11-20 of 1,418) with videos related to
Sort By:
Pageof 142
Journal of Medical Genetics|November 1, 1995
Pfeiffer type cardiocranial syndrome: a third case reportL Williamson-Kruse, L G BieseckerAmerican Journal of Medical Genetics|September 1, 1987
Renal insufficiency in Williams syndromeL G Biesecker, R Laxova, A FriedmanAmerican Journal of Medical Genetics|September 15, 1991
Severe anomalies associated with ring chromosome 7L G Biesecker, B Cox, T W GloverBiochemical Medicine and Metabolic Biology|February 1, 1994
Bone marrow transplantation demonstrates that carbonic anhydrase II deficiency limited to bone marrow-derived cells affects ammonium chloride tolerance in miceL G Biesecker, R P Erickson, R E TashianProceedings of the National Academy of Sciences of the United States of America|August 1, 1993
Identification of four murine cDNAs encoding putative protein kinases from primitive embryonic stem cells differentiated in vitroL G Biesecker, L R Gottschalk, S G EmersonJournal of Computational Biology : a Journal of Computational Molecular Cell Biology|May 16, 1998
Approximation algorithms for a genetic diagnostics problemS R Kosaraju, A A Schäffer, L G BieseckerOncogene|June 1, 1995
Identification of alternative exons, including a novel exon, in the tyrosine kinase receptor gene Etk2/tyro3 that explain differences in 5' cDNA sequencesL G Biesecker, D M Giannola, S G EmersonAmerican Journal of Medical Genetics|September 25, 2001
Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromesE T Rosenthal, L G Biesecker, B B BieseckerAmerican Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.Journal of Medical Genetics|July 1, 1993
Mild phenotypic manifestation of a 7p15.3p21.2 deletionC Wang, S Maynard, T W Glover, et al.Pageof 142