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Genetic Testing
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February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findings
C Fridman, M C Varela, F Kok, et al.
Genetic Testing
|
February 24, 2001
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations
G Loudianos, M Lovicu, P Solinas, et al.
Genetic Testing
|
February 24, 2001
Disease genes and chromosomes: disease maps of the human genome
F Gilbert
Genetic Testing
|
October 24, 2007
The use of ancestral haplotypes in the molecular diagnosis of familial breast cancer
Patrick Frosk, Susan Burgess, Tamara Dyck, et al.
Genetic Testing
|
October 24, 2007
Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish patient with beta-thalassemia major
Ibrahim Keser, Esra Manguoglu, Ozlem Kayisli, et al.
Genetic Testing
|
October 24, 2007
Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay
Satoko Abe, Toshikazu Yamaguchi, Shin-Ichi Usami
Genetic Testing
|
March 21, 2006
Genetic Testing for Huntington's Disease: How Is the Decision Taken?
Holly Etchegary
Genetic Testing
|
March 21, 2006
A fluorescent multiplex-DGGE screening test for mutations in the BRCA1 gene
Graciela Kuperstein, Elaine Jack, Steven A Narod
Genetic Testing
|
March 21, 2006
Screening of Nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers
Alessandra Di Masi, Antonio Antoccia, Emanuela Spadoni, et al.
Genetic Testing
|
March 21, 2006
Predictors of belief that genetic test information about hemochromatosis should be shared with family members
Diane C Tucker, Ronald T Acton, Nancy Press, et al.
Page
of 68
Search research articles
Search
Showing results (101-110 of 679) with videos related to
Sort By:
Page
of 68
Genetic Testing
|
February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findings
C Fridman, M C Varela, F Kok, et al.
Genetic Testing
|
February 24, 2001
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations
G Loudianos, M Lovicu, P Solinas, et al.
Genetic Testing
|
February 24, 2001
Disease genes and chromosomes: disease maps of the human genome
F Gilbert
Genetic Testing
|
October 24, 2007
The use of ancestral haplotypes in the molecular diagnosis of familial breast cancer
Patrick Frosk, Susan Burgess, Tamara Dyck, et al.
Genetic Testing
|
October 24, 2007
Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish patient with beta-thalassemia major
Ibrahim Keser, Esra Manguoglu, Ozlem Kayisli, et al.
Genetic Testing
|
October 24, 2007
Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay
Satoko Abe, Toshikazu Yamaguchi, Shin-Ichi Usami
Genetic Testing
|
March 21, 2006
Genetic Testing for Huntington's Disease: How Is the Decision Taken?
Holly Etchegary
Genetic Testing
|
March 21, 2006
A fluorescent multiplex-DGGE screening test for mutations in the BRCA1 gene
Graciela Kuperstein, Elaine Jack, Steven A Narod
Genetic Testing
|
March 21, 2006
Screening of Nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers
Alessandra Di Masi, Antonio Antoccia, Emanuela Spadoni, et al.
Genetic Testing
|
March 21, 2006
Predictors of belief that genetic test information about hemochromatosis should be shared with family members
Diane C Tucker, Ronald T Acton, Nancy Press, et al.
Page
of 68