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J S Waye

Showing results (41-50 of 115) with videos related to

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Human Mutation|January 1, 1995
Novel seventeen basepair deletion in exon 3 of the beta-globin geneJ S Waye, B Eng, W H Francombe, et al.
Journal of Forensic Sciences|July 1, 1991
Sensitive and specific quantification of human genomic deoxyribonucleic acid (DNA) in forensic science specimens: casework examplesJ S Waye, D Michaud, J H Bowen, et al.
Prenatal Diagnosis|October 1, 1994
Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosisJ S Waye, B Eng, N F Olivieri, et al.
American Journal of Medical Genetics|August 15, 2001
Rapid molecular prenatal diagnosis of Smith-Lemli-Opitz syndromeM J Nowaczyk, D M Garcia, B Eng, et al.
Human Genetics|November 1, 1994
Filipino beta-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosisJ S Waye, B Eng, J A Hunt, et al.
Journal of Forensic Sciences|May 1, 1990
Hae III--a suitable restriction endonuclease for restriction fragment length polymorphism analysis of biological evidence samplesB Budowle, J S Waye, G G Shutler, et al.
Genomics|December 1, 1987
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosisH F Willard, G M Greig, V E Powers, et al.
American Journal of Clinical Pathology|May 8, 2001
A reliable screening test to identify adult carriers of the (--SEA) alpha zero-thalassemia deletion. Detection of embryonic zeta-globin chains by enzyme-linked immunosorbent assayJ D Lafferty, M A Crowther, J S Waye, et al.
Hemoglobin|February 24, 2001
Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H diseaseJ S Waye, L Walker, D H Chui, et al.
Genetic Testing|April 19, 2002
Detection of severe nondeletional alpha-thalassemia mutations using a single-tube multiplex ARMS assayB Eng, M Patterson, L Walker, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
Human Mutation|January 1, 1995
Novel seventeen basepair deletion in exon 3 of the beta-globin geneJ S Waye, B Eng, W H Francombe, et al.
Journal of Forensic Sciences|July 1, 1991
Sensitive and specific quantification of human genomic deoxyribonucleic acid (DNA) in forensic science specimens: casework examplesJ S Waye, D Michaud, J H Bowen, et al.
Prenatal Diagnosis|October 1, 1994
Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosisJ S Waye, B Eng, N F Olivieri, et al.
American Journal of Medical Genetics|August 15, 2001
Rapid molecular prenatal diagnosis of Smith-Lemli-Opitz syndromeM J Nowaczyk, D M Garcia, B Eng, et al.
Human Genetics|November 1, 1994
Filipino beta-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosisJ S Waye, B Eng, J A Hunt, et al.
Journal of Forensic Sciences|May 1, 1990
Hae III--a suitable restriction endonuclease for restriction fragment length polymorphism analysis of biological evidence samplesB Budowle, J S Waye, G G Shutler, et al.
Genomics|December 1, 1987
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosisH F Willard, G M Greig, V E Powers, et al.
American Journal of Clinical Pathology|May 8, 2001
A reliable screening test to identify adult carriers of the (--SEA) alpha zero-thalassemia deletion. Detection of embryonic zeta-globin chains by enzyme-linked immunosorbent assayJ D Lafferty, M A Crowther, J S Waye, et al.
Hemoglobin|February 24, 2001
Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H diseaseJ S Waye, L Walker, D H Chui, et al.
Genetic Testing|April 19, 2002
Detection of severe nondeletional alpha-thalassemia mutations using a single-tube multiplex ARMS assayB Eng, M Patterson, L Walker, et al.
Pageof 12