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American Journal of Medical Genetics|August 17, 1999
Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric regionE Holinski-Feder, S Chahrockh-Zadeh, O Rittinger, et al.
American Journal of Medical Genetics|May 3, 1996
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7pS von Gernet, S Schuffenhauer, A Golla, et al.
Clinical Genetics|January 24, 1998
Detection of 100% of the CFTR mutations in 63 CF families from TyrolM Stuhrmann, T Dörk, M Frühwirth, et al.
Macromolecules|March 2, 2026
The Importance of Branch Placement on the Dilute Solution Properties of Comb-like MacromoleculesRobert J S Ivancic, Chase B Thompson, Devin A Golla, et al.
American Journal of Human Genetics|June 1, 1992
Evidence for genetic heterogeneity of malignant hyperthermia susceptibilityT Deufel, A Golla, D Iles, et al.
Journal of the American Medical Directors Association|January 12, 2021
Effects of Unstructured Mobility Programs in Older Hospitalized General Medicine Patients: A Systematic Review and Meta-AnalysisCourtney D Reynolds, Kaitlyn V Brazier, Evelyn A A Burgess, et al.
The Review of Scientific Instruments|April 5, 2011
Lost in reciprocal space? Determination of the scattering condition in spot profile analysis low-energy electron diffractionC Klein, T Nabbefeld, H Hattab, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 15, 2026
Precision A3G Base Editors for Disease Modeling and CorrectionHongzhi Zeng, Aidi Liu, Tyler C Daniel, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
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