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C Kaplan

Showing results (571-580 of 1,185) with videos related to

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Annales De Genetique|January 9, 1999
Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileusJ Steffann, D Vidaud, S Bousquet, et al.
Clinical Genetics|January 1, 1997
Spectrum of CFTR mutations in Argentine cystic fibrosis patientsL Chertkoff, A Visich, T Bienvenu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1992
Intrapulmonary neuroglial heterotopiaM M Kershisnik, C Kaplan, C M Craven, et al.
Thrombosis Research|November 5, 2002
Elevated levels of Factor XI are associated with cardiovascular disease in womenJennifer I Berliner, Anne C Rybicki, Robert C Kaplan, et al.
Human Mutation|January 1, 1995
Screening for mutations in factor VIII gene using the single-strand conformation polymorphismK Nafa, F Meriane, T Chellali, et al.
Nucleic Acids Research|July 11, 1991
Maximizing sensitivity and specificity of PCR by pre-amplification heatingR T D'Aquila, L J Bechtel, J A Videler, et al.
BMJ Quality & Safety|June 10, 2015
Reliable implementation of evidence: a qualitative study of antenatal corticosteroid administration in Ohio hospitalsHeather C Kaplan, Susan N Sherman, Charlena Cleveland, et al.
Human Genetics|January 1, 1980
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalanceC Junien, H Rubinson-Skala, J C Dreyfus, et al.
American Journal of Human Genetics|July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2I Henry, G Uzan, D Weil, et al.
Pageof 119

Showing results (571-580 of 1,185) with videos related to

Sort By:
Pageof 119
Annales De Genetique|January 9, 1999
Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileusJ Steffann, D Vidaud, S Bousquet, et al.
Clinical Genetics|January 1, 1997
Spectrum of CFTR mutations in Argentine cystic fibrosis patientsL Chertkoff, A Visich, T Bienvenu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1992
Intrapulmonary neuroglial heterotopiaM M Kershisnik, C Kaplan, C M Craven, et al.
Thrombosis Research|November 5, 2002
Elevated levels of Factor XI are associated with cardiovascular disease in womenJennifer I Berliner, Anne C Rybicki, Robert C Kaplan, et al.
Human Mutation|January 1, 1995
Screening for mutations in factor VIII gene using the single-strand conformation polymorphismK Nafa, F Meriane, T Chellali, et al.
Nucleic Acids Research|July 11, 1991
Maximizing sensitivity and specificity of PCR by pre-amplification heatingR T D'Aquila, L J Bechtel, J A Videler, et al.
BMJ Quality & Safety|June 10, 2015
Reliable implementation of evidence: a qualitative study of antenatal corticosteroid administration in Ohio hospitalsHeather C Kaplan, Susan N Sherman, Charlena Cleveland, et al.
Human Genetics|January 1, 1980
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalanceC Junien, H Rubinson-Skala, J C Dreyfus, et al.
American Journal of Human Genetics|July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2I Henry, G Uzan, D Weil, et al.
Pageof 119