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Clinical Genetics
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August 31, 1999
Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations
M R Eccles, L A Schimmenti
Clinical Genetics
|
August 31, 1999
Family physicians' perspectives on genetics and the human genome project
M D Fetters, D J Doukas, K L Phan
Clinical Genetics
|
August 31, 1999
Cohen syndrome: evaluation of its cardiac, endocrine and radiological features
S 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 activity
G 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 history
P 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 10p
S A Berend, L G Shaffer, B A Bejjani
Clinical Genetics
|
September 27, 2000
Intrachromosomal triplications: molecular cytogenetic and clinical studies
K S Reddy, J J Logan
Clinical Genetics
|
March 1, 1975
A computer-oriented linkage analysis scheme
L B Freidhoff, G Chase
Clinical Genetics
|
May 1, 1975
A simple combinatorial method for calculating genetic risks
U R Maag, R J Gold
Page
of 718
Search research articles
Search
Showing results (571-580 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
August 31, 1999
Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations
M R Eccles, L A Schimmenti
Clinical Genetics
|
August 31, 1999
Family physicians' perspectives on genetics and the human genome project
M D Fetters, D J Doukas, K L Phan
Clinical Genetics
|
August 31, 1999
Cohen syndrome: evaluation of its cardiac, endocrine and radiological features
S 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 activity
G 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 history
P 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 10p
S A Berend, L G Shaffer, B A Bejjani
Clinical Genetics
|
September 27, 2000
Intrachromosomal triplications: molecular cytogenetic and clinical studies
K S Reddy, J J Logan
Clinical Genetics
|
March 1, 1975
A computer-oriented linkage analysis scheme
L B Freidhoff, G Chase
Clinical Genetics
|
May 1, 1975
A simple combinatorial method for calculating genetic risks
U R Maag, R J Gold
Page
of 718