Showing results (191-200 of 199) with videos related to
Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 199 results.
American Journal of Human Genetics|December 1, 1995
Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemiaT M Narcisi, C C Shoulders, S A Chester, et al.American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.American Journal of Human Genetics|July 6, 2000
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderC S Lai, S E Fisher, J A Hurst, et al.Annals of Human Genetics|May 1, 1997
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996S Povey, J Attwood, B Chadwick, et al.Annals of Human Genetics|November 1, 1996
European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme HumainS A Cox, J Attwood, S P Bryant, et al.Human Mutation|December 25, 2007
Recommendations for locus-specific databases and their curationR G H Cotton, A D Auerbach, J S Beckmann, et al.Journal of Community Genetics|September 16, 2018
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwideSowmiya Moorthie, Hannah Blencowe, Matthew W Darlison, et al.Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.Nature|May 28, 2004
DNA sequence and analysis of human chromosome 9S J Humphray, K Oliver, A R Hunt, et al.Pageof 20