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B Eng

Showing results (41-50 of 99) with videos related to

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Human Genetics|October 1, 1991
A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to beta-thalassemiaS P Cai, B Eng, Y W Kan, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 1, 1992
The effects of nasal dilation on snoring and obstructive sleep apneaU Höijer, H Ejnell, J Hedner, 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.
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.
American Journal of Hematology|December 22, 1999
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletionsB Eng, M Patterson, S Borys, et al.
American Journal of Medical Genetics|April 12, 2001
DHCR7 genotypes of cousins with Smith-Lemli-Opitz syndromeM J Nowaczyk, T Heshka, B Eng, et al.
Molecular and Cellular Probes|April 1, 1994
Trinucleotide repeat polymorphism within the human antithrombin gene (AT3): allele frequency data for three population groupsJ S Waye, B Eng, H Y Ni, et al.
Human Mutation|January 1, 1993
Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletionB Eng, D H Chui, J Saunderson, et al.
Hemoglobin|July 1, 1997
Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T)J S Waye, B Eng, M Patterson, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
Human Genetics|October 1, 1991
A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to beta-thalassemiaS P Cai, B Eng, Y W Kan, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 1, 1992
The effects of nasal dilation on snoring and obstructive sleep apneaU Höijer, H Ejnell, J Hedner, 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.
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.
American Journal of Hematology|December 22, 1999
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletionsB Eng, M Patterson, S Borys, et al.
American Journal of Medical Genetics|April 12, 2001
DHCR7 genotypes of cousins with Smith-Lemli-Opitz syndromeM J Nowaczyk, T Heshka, B Eng, et al.
Molecular and Cellular Probes|April 1, 1994
Trinucleotide repeat polymorphism within the human antithrombin gene (AT3): allele frequency data for three population groupsJ S Waye, B Eng, H Y Ni, et al.
Human Mutation|January 1, 1993
Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletionB Eng, D H Chui, J Saunderson, et al.
Hemoglobin|July 1, 1997
Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T)J S Waye, B Eng, M Patterson, et al.
Pageof 10