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D N Cooper

Showing results (191-200 of 205) with videos related to

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Human Genetics|February 1, 1987
Regional localization and characterization of a DNA segment on the long arm of chromosome 21D N Cooper, S C Niemann, J R Gosden, et al.
The Journal of Biological Chemistry|March 10, 1995
Sequence and mapping of galectin-5, a beta-galactoside-binding lectin, found in rat erythrocytesM A Gitt, M F Wiser, H Leffler, et al.
Human Genetics|July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delayM Upadhyaya, M Ruggieri, J Maynard, et al.
Human Molecular Genetics|September 1, 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VIIO Takamiya, G Kemball-Cook, D M Martin, et al.
Human Pathology|November 1, 1996
Expression of the 67-kD laminin receptor, galectin-1, and galectin-3 in advanced human uterine adenocarcinomaF A van den Brule, C Buicu, A Berchuck, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Thrombosis and Haemostasis|January 1, 1997
Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisD A Lane, T Bayston, R J Olds, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Blood|October 1, 1995
Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategyC J Formstone, A I Wacey, L P Berg, et al.
Thrombosis and Haemostasis|December 29, 2000
Protein S deficiency: a database of mutations--summary of the first updateS Gandrille, D Borgel, N Sala, et al.
Pageof 21

Showing results (191-200 of 205) with videos related to

Sort By:
Pageof 21
Human Genetics|February 1, 1987
Regional localization and characterization of a DNA segment on the long arm of chromosome 21D N Cooper, S C Niemann, J R Gosden, et al.
The Journal of Biological Chemistry|March 10, 1995
Sequence and mapping of galectin-5, a beta-galactoside-binding lectin, found in rat erythrocytesM A Gitt, M F Wiser, H Leffler, et al.
Human Genetics|July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delayM Upadhyaya, M Ruggieri, J Maynard, et al.
Human Molecular Genetics|September 1, 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VIIO Takamiya, G Kemball-Cook, D M Martin, et al.
Human Pathology|November 1, 1996
Expression of the 67-kD laminin receptor, galectin-1, and galectin-3 in advanced human uterine adenocarcinomaF A van den Brule, C Buicu, A Berchuck, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Thrombosis and Haemostasis|January 1, 1997
Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisD A Lane, T Bayston, R J Olds, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Blood|October 1, 1995
Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategyC J Formstone, A I Wacey, L P Berg, et al.
Thrombosis and Haemostasis|December 29, 2000
Protein S deficiency: a database of mutations--summary of the first updateS Gandrille, D Borgel, N Sala, et al.
Pageof 21