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J S Waye

Showing results (51-60 of 115) with videos related to

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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.
Gene|January 1, 1985
Nonrandom insertion of Tn5 into cloned human adenovirus DNAR D McKinnon, J S Waye, D S Bautista, 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.
Hemoglobin|March 11, 1998
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)]J S Waye, B Eng, M Patterson, et al.
American Journal of Medical Genetics|March 1, 1993
Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiencyN Shen, Z G Li, J S Waye, et al.
Hemoglobin|January 1, 1995
Identification of a new high oxygen affinity hemoglobin variant: Hb Aurora [beta 139(H17) Asn-->Tyr]J Lafferty, M Ali, K Matthew, et al.
Blood|June 1, 1994
Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H diseaseJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|November 26, 1997
De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European boyJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|June 1, 1994
Genetic linkage studies in antithrombin-deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (STR) within the human antithrombin geneH Ni, J S Waye, W P Sheffield, 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.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
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.
Gene|January 1, 1985
Nonrandom insertion of Tn5 into cloned human adenovirus DNAR D McKinnon, J S Waye, D S Bautista, 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.
Hemoglobin|March 11, 1998
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)]J S Waye, B Eng, M Patterson, et al.
American Journal of Medical Genetics|March 1, 1993
Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiencyN Shen, Z G Li, J S Waye, et al.
Hemoglobin|January 1, 1995
Identification of a new high oxygen affinity hemoglobin variant: Hb Aurora [beta 139(H17) Asn-->Tyr]J Lafferty, M Ali, K Matthew, et al.
Blood|June 1, 1994
Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H diseaseJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|November 26, 1997
De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European boyJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|June 1, 1994
Genetic linkage studies in antithrombin-deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (STR) within the human antithrombin geneH Ni, J S Waye, W P Sheffield, 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.
Pageof 12