Showing results (671-680 of 9,786) with videos related to
Sort By:
Pageof 979
American Journal of Human Genetics|January 1, 1984
An evaluation of three statistics of structured exploratory data analysisC M Kammerer, J W MacCluer, J M BridgesAmerican Journal of Human Genetics|January 1, 1984
Isolation of repetitive DNA sequences from human chromosome 21G J Graham, T J Hall, M R CummingsAmerican Journal of Human Genetics|March 1, 1995
A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotypeM Chillón, T Dörk, T Casals, et al.American Journal of Human Genetics|June 1, 1995
Mutations in the SLC3A1 transporter gene in cystinuriaE Pras, N Raben, E Golomb, et al.American Journal of Human Genetics|January 1, 1978
Combination of silver and fluorescent staining for metaphase chromosomesY F Lau, R A Pfeiffer, F E Arrighi, et al.American Journal of Human Genetics|December 1, 1993
Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry diseaseC M Eng, L A Resnick-Silverman, D J Niehaus, et al.American Journal of Human Genetics|October 1, 1995
An amino acid substitution in the pyruvate dehydrogenase E1 alpha gene, affecting mitochondrial import of the precursor proteinF Takakubo, P Cartwright, N Hoogenraad, et al.American Journal of Human Genetics|October 1, 1995
Genetic mapping of the dentinogenesis imperfecta type II locusA H Crosby, T Scherpbier-Heddema, C Wijmenga, et al.American Journal of Human Genetics|October 1, 1995
Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study GroupM Krajinovic, B Pinamonti, G Sinagra, et al.American Journal of Human Genetics|October 1, 1995
Genetic analysis of kifafa, a complex familial seizure disorderR J Neuman, J M Kwon, L Jilek-Aall, et al.Pageof 979