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Clinical Genetics
|
September 14, 2007
The genetics of mitral valve prolapse
J B Grau, L Pirelli, P-J Yu, et al.
Clinical Genetics
|
March 18, 2004
The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects
T Fitzgerald, S Duva, H Ostrer, et al.
Annals of the New York Academy of Sciences
|
January 1, 1984
Isolation of cDNA clones for rabbit red cell carbonic anhydrase and catalase: a pilot study directed at isolation of coordinately expressed genes
S H Boyer, H Ostrer, K D Smith, et al.
Genomics
|
May 1, 1989
Localization of the human type 5, tartrate-resistant acid phosphatase gene by in situ hybridization
B S Allen, C M Ketcham, R M Roberts, et al.
Prenatal Diagnosis
|
February 1, 1990
Establishment of a cytogenetic service for chorionic villus samples: the split specimen approach
E S Cantú, H Ostrer, B A Gray, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Relationship of autoimmunity to thyroid dysfunction in children and adults with Down syndrome
R T Zori, D A Schatz, H Ostrer, et al.
The Journal of Laryngology and Otology
|
September 18, 2014
Bioinformatics in otolaryngology research. Part two: other high-throughput platforms in genomics and epigenetics
T J Ow, K Upadhyay, T J Belbin, et al.
Journal of Medical Genetics
|
September 11, 1998
Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?
A S Teebi, S Miller, H Ostrer, et al.
Prenatal Diagnosis
|
September 1, 1995
Prenatal diagnostic testing for familial dysautonomia using linked genetic markers
C Oddoux, E Reich, F Axelrod, et al.
The Journal of Laryngology and Otology
|
September 17, 2014
Bioinformatics in otolaryngology research. Part one: concepts in DNA sequencing and gene expression analysis
T J Ow, K Upadhyay, T J Belbin, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 83) with videos related to
Sort By:
Page
of 9
Clinical Genetics
|
September 14, 2007
The genetics of mitral valve prolapse
J B Grau, L Pirelli, P-J Yu, et al.
Clinical Genetics
|
March 18, 2004
The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects
T Fitzgerald, S Duva, H Ostrer, et al.
Annals of the New York Academy of Sciences
|
January 1, 1984
Isolation of cDNA clones for rabbit red cell carbonic anhydrase and catalase: a pilot study directed at isolation of coordinately expressed genes
S H Boyer, H Ostrer, K D Smith, et al.
Genomics
|
May 1, 1989
Localization of the human type 5, tartrate-resistant acid phosphatase gene by in situ hybridization
B S Allen, C M Ketcham, R M Roberts, et al.
Prenatal Diagnosis
|
February 1, 1990
Establishment of a cytogenetic service for chorionic villus samples: the split specimen approach
E S Cantú, H Ostrer, B A Gray, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Relationship of autoimmunity to thyroid dysfunction in children and adults with Down syndrome
R T Zori, D A Schatz, H Ostrer, et al.
The Journal of Laryngology and Otology
|
September 18, 2014
Bioinformatics in otolaryngology research. Part two: other high-throughput platforms in genomics and epigenetics
T J Ow, K Upadhyay, T J Belbin, et al.
Journal of Medical Genetics
|
September 11, 1998
Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?
A S Teebi, S Miller, H Ostrer, et al.
Prenatal Diagnosis
|
September 1, 1995
Prenatal diagnostic testing for familial dysautonomia using linked genetic markers
C Oddoux, E Reich, F Axelrod, et al.
The Journal of Laryngology and Otology
|
September 17, 2014
Bioinformatics in otolaryngology research. Part one: concepts in DNA sequencing and gene expression analysis
T J Ow, K Upadhyay, T J Belbin, et al.
Page
of 9