Search research articles
Contact Us
Filters
Showing results (31-40 of 77) with videos related to
Page
of 8
Sort By:
Clinical Genetics
|
May 20, 2003
Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes
M Tartaglia, P D Cotter, G Zampino, et al.
American Journal of Medical Genetics
|
August 5, 2000
Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome
K A Rauen, P D Cotter, S M Bitts, et al.
Genomics
|
February 1, 1997
Physical mapping of the human connexin 40 (GJA5), flavin-containing monooxygenase 5, and natriuretic peptide receptor a genes on 1q21
B D Gelb, J Zhang, P D Cotter, et al.
Clinical Genetics
|
January 10, 2001
Segregation of a supernumerary del(15) marker chromosome in sperm
P D Cotter, E Ko, S K Larabell, et al.
Probiotics and Antimicrobial Proteins
|
September 25, 2017
Lack of Heterogeneity in Bacteriocin Production Across a Selection of Commercial Probiotic Products
J W Hegarty, C M Guinane, R P Ross, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Assignment of the human housekeeping delta-aminolevulinate synthase gene (ALAS1) to chromosome band 3p21.1 by PCR analysis of somatic cell hybrids
P D Cotter, H A Drabkin, T Varkony, et al.
American Journal of Medical Genetics
|
May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and review
P D Cotter, S Kaffe, L D McCurdy, et al.
Cancer Genetics and Cytogenetics
|
April 5, 2000
Monosomy 16 as the sole abnormality in myeloid malignancies
E M McGhee, N R Cohen, J L Wolf, et al.
Clinical Dysmorphology
|
April 20, 2001
Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome
E J Lammer, D R Punglia, A E Fuchs, et al.
American Journal of Medical Genetics
|
August 5, 2000
Candidate region for Coffin-Siris syndrome at 7q32-->34
E M McGhee, C J Klump, S M Bitts, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Clinical Genetics
|
May 20, 2003
Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes
M Tartaglia, P D Cotter, G Zampino, et al.
American Journal of Medical Genetics
|
August 5, 2000
Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome
K A Rauen, P D Cotter, S M Bitts, et al.
Genomics
|
February 1, 1997
Physical mapping of the human connexin 40 (GJA5), flavin-containing monooxygenase 5, and natriuretic peptide receptor a genes on 1q21
B D Gelb, J Zhang, P D Cotter, et al.
Clinical Genetics
|
January 10, 2001
Segregation of a supernumerary del(15) marker chromosome in sperm
P D Cotter, E Ko, S K Larabell, et al.
Probiotics and Antimicrobial Proteins
|
September 25, 2017
Lack of Heterogeneity in Bacteriocin Production Across a Selection of Commercial Probiotic Products
J W Hegarty, C M Guinane, R P Ross, et al.
Cytogenetics and Cell Genetics
|
January 1, 1995
Assignment of the human housekeeping delta-aminolevulinate synthase gene (ALAS1) to chromosome band 3p21.1 by PCR analysis of somatic cell hybrids
P D Cotter, H A Drabkin, T Varkony, et al.
American Journal of Medical Genetics
|
May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and review
P D Cotter, S Kaffe, L D McCurdy, et al.
Cancer Genetics and Cytogenetics
|
April 5, 2000
Monosomy 16 as the sole abnormality in myeloid malignancies
E M McGhee, N R Cohen, J L Wolf, et al.
Clinical Dysmorphology
|
April 20, 2001
Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome
E J Lammer, D R Punglia, A E Fuchs, et al.
American Journal of Medical Genetics
|
August 5, 2000
Candidate region for Coffin-Siris syndrome at 7q32-->34
E M McGhee, C J Klump, S M Bitts, et al.
Page
of 8