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Genetic testing

Showing results (281-290 of 679) with videos related to

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Genetic Testing|March 1, 2008
Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndromeKatja Eggermann, Nadine Schönherr, Michael B Ranke, et al.
Genetic Testing|March 1, 2008
An anomalous haplotype distribution of the arrestin domain-containing 4 gene (ARRDC4) haplotypes in CaucasiansBettina Knoll, Mark Goldammer, Agnieszka Wojewoda, et al.
Genetic Testing|October 6, 2006
Systematic analysis of sequence variability of the endothelin-1 gene: a prerequisite for association studiesKonstanze Diefenbach, Farhad Arjomand-Nahad, Christian Meisel, et al.
Genetic Testing|October 6, 2006
Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocolsS Giannattasio, A Bobba, V Jurgelevicius, et al.
Genetic Testing|October 6, 2006
Robust, easy, and dose-sensitive methylation test for the diagnosis of Prader-Willi and Angelman syndromesFrancisco Martínez, Ana María León, Sandra Monfort, et al.
Genetic Testing|October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's diseaseDenise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Genetic Testing|August 1, 2008
Bilateral transverse sinus thrombosis secondary to a homozygous C677T MTHFR gene mutationZiad M Kanaan, Rami Mahfouz, Ali Taher, et al.
Genetic Testing|July 26, 2008
Estimation of Wilson's disease incidence and carrier frequency in the Korean population by screening ATP7B major mutations in newborn filter papers using the SYBR green intercalator method based on the amplification refractory mutation systemGu-Hwan Kim, Jeong Yoon Yang, Jung-Young Park, et al.
Genetic Testing|July 26, 2008
The CFTR M470V gene variant as a potential modifier of COPD severity: study of Serbian populationMarija Stankovic, Aleksandra Nikolic, Aleksandra Divac, et al.
Genetic Testing|July 17, 2008
Complement factor H variant p.Y402H in pseudoxanthoma elasticum patientsChristian Götting, Doris Hendig, Ralf Zarbock, et al.
Pageof 68

Showing results (281-290 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|March 1, 2008
Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndromeKatja Eggermann, Nadine Schönherr, Michael B Ranke, et al.
Genetic Testing|March 1, 2008
An anomalous haplotype distribution of the arrestin domain-containing 4 gene (ARRDC4) haplotypes in CaucasiansBettina Knoll, Mark Goldammer, Agnieszka Wojewoda, et al.
Genetic Testing|October 6, 2006
Systematic analysis of sequence variability of the endothelin-1 gene: a prerequisite for association studiesKonstanze Diefenbach, Farhad Arjomand-Nahad, Christian Meisel, et al.
Genetic Testing|October 6, 2006
Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocolsS Giannattasio, A Bobba, V Jurgelevicius, et al.
Genetic Testing|October 6, 2006
Robust, easy, and dose-sensitive methylation test for the diagnosis of Prader-Willi and Angelman syndromesFrancisco Martínez, Ana María León, Sandra Monfort, et al.
Genetic Testing|October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's diseaseDenise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Genetic Testing|August 1, 2008
Bilateral transverse sinus thrombosis secondary to a homozygous C677T MTHFR gene mutationZiad M Kanaan, Rami Mahfouz, Ali Taher, et al.
Genetic Testing|July 26, 2008
Estimation of Wilson's disease incidence and carrier frequency in the Korean population by screening ATP7B major mutations in newborn filter papers using the SYBR green intercalator method based on the amplification refractory mutation systemGu-Hwan Kim, Jeong Yoon Yang, Jung-Young Park, et al.
Genetic Testing|July 26, 2008
The CFTR M470V gene variant as a potential modifier of COPD severity: study of Serbian populationMarija Stankovic, Aleksandra Nikolic, Aleksandra Divac, et al.
Genetic Testing|July 17, 2008
Complement factor H variant p.Y402H in pseudoxanthoma elasticum patientsChristian Götting, Doris Hendig, Ralf Zarbock, et al.
Pageof 68