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Clinical genetics

Showing results (571-580 of 7,173) with videos related to

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Clinical Genetics|August 31, 1999
Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutationsM R Eccles, L A Schimmenti
Clinical Genetics|August 31, 1999
Family physicians' perspectives on genetics and the human genome projectM D Fetters, D J Doukas, K L Phan
Clinical Genetics|August 31, 1999
Cohen syndrome: evaluation of its cardiac, endocrine and radiological featuresS Kivitie-Kallio, M Eronen, M Lipsanen-Nyman, et al.
Clinical Genetics|August 31, 1999
Mucopolysaccharidosis type I: characterization of novel mutations affecting alpha-L-iduronidase activityG J Lee-Chen, S P Lin, Y F Tang, et al.
Clinical Genetics|July 28, 1999
Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family historyP N Tonin, A M Mes-Masson, S A Narod, et al.
Clinical Genetics|July 28, 1999
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)U Ekström, M Abrahamson, C H Florén, et al.
Clinical Genetics|July 28, 1999
Pure trisomy 10p involving an isochromosome 10pS A Berend, L G Shaffer, B A Bejjani
Clinical Genetics|September 27, 2000
Intrachromosomal triplications: molecular cytogenetic and clinical studiesK S Reddy, J J Logan
Clinical Genetics|March 1, 1975
A computer-oriented linkage analysis schemeL B Freidhoff, G Chase
Clinical Genetics|May 1, 1975
A simple combinatorial method for calculating genetic risksU R Maag, R J Gold
Pageof 718

Showing results (571-580 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|August 31, 1999
Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutationsM R Eccles, L A Schimmenti
Clinical Genetics|August 31, 1999
Family physicians' perspectives on genetics and the human genome projectM D Fetters, D J Doukas, K L Phan
Clinical Genetics|August 31, 1999
Cohen syndrome: evaluation of its cardiac, endocrine and radiological featuresS Kivitie-Kallio, M Eronen, M Lipsanen-Nyman, et al.
Clinical Genetics|August 31, 1999
Mucopolysaccharidosis type I: characterization of novel mutations affecting alpha-L-iduronidase activityG J Lee-Chen, S P Lin, Y F Tang, et al.
Clinical Genetics|July 28, 1999
Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family historyP N Tonin, A M Mes-Masson, S A Narod, et al.
Clinical Genetics|July 28, 1999
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)U Ekström, M Abrahamson, C H Florén, et al.
Clinical Genetics|July 28, 1999
Pure trisomy 10p involving an isochromosome 10pS A Berend, L G Shaffer, B A Bejjani
Clinical Genetics|September 27, 2000
Intrachromosomal triplications: molecular cytogenetic and clinical studiesK S Reddy, J J Logan
Clinical Genetics|March 1, 1975
A computer-oriented linkage analysis schemeL B Freidhoff, G Chase
Clinical Genetics|May 1, 1975
A simple combinatorial method for calculating genetic risksU R Maag, R J Gold
Pageof 718