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Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.Genomics|August 1, 1992
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionA M van den Ouweland, M T Knoop, V V Knoers, et al.Genomics|December 1, 1987
Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1)M A Pericak-Vance, L H Yamaoka, J M Vance, et al.American Journal of Human Genetics|January 1, 1989
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type IJ M Vance, M A Pericak-Vance, L H Yamaoka, et al.Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.Clinical Obesity|February 22, 2023
Clinical characteristics of patients undergoing primary bariatric surgery in the United Kingdom based on the National Bariatric Surgery RegistryRoel Bolckmans, Alan Askari, Andrew Currie, et al.Journal of Thrombosis and Haemostasis : JTH|July 15, 2006
Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural geneM Khachidze, A Buil, K R Viel, et al.Leukemia|February 25, 2015
Dinaciclib is a novel cyclin-dependent kinase inhibitor with significant clinical activity in relapsed and refractory chronic lymphocytic leukemiaJ Flynn, J Jones, A J Johnson, et al.Obesity Surgery|December 16, 2017
The First Consensus Statement on One Anastomosis/Mini Gastric Bypass (OAGB/MGB) Using a Modified Delphi ApproachKamal K Mahawar, Jacques Himpens, Scott A Shikora, et al.American Journal of Human Genetics|March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.Pageof 20