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Orphanet Journal of Rare Diseases|April 26, 2008
The Greig cephalopolysyndactyly syndromeLeslie G BieseckerAmerican Journal of Human Genetics|May 7, 2013
Incidental variants are critical for genomicsLeslie G BieseckerGenome Research|July 3, 2013
Hypothesis-generating research and predictive medicineLeslie G BieseckerAmerican Journal of Medical Genetics. Part A|November 26, 2013
Invited editorial comment--The human phenotype of germline PIGA mutationsLeslie G BieseckerAmerican Journal of Medical Genetics. Part A|February 5, 2008
The clinical atlas of Greig cephalopolysyndactyly syndromeKatherine Balk, Leslie G BieseckerAmerican Journal of Medical Genetics. Part A|August 17, 2005
No evidence for triallelic inheritance of MKKS/BBS loci in Amish Mckusick-Kaufman syndromeTakaya Nakane, Leslie G BieseckerHuman Molecular Genetics|April 2, 2003
Genetic modifiers in human development and malformation syndromes, including chaperone proteinsAnne Slavotinek, Leslie G BieseckerNature Reviews. Genetics|April 19, 2013
A genomic view of mosaicism and human diseaseLeslie G Biesecker, Nancy B SpinnerHuman Molecular Genetics|August 22, 2013
Databases of genomic variation and phenotypes: existing resources and future needsJennifer J Johnston, Leslie G BieseckerCurrent Opinion in Pediatrics|October 12, 2014
An approach to pediatric exome and genome sequencingLeslie G Biesecker, Barbara B BieseckerPageof 32