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B D Gelb

Showing results (31-40 of 76) with videos related to

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Journal of Human Genetics|September 25, 1999
Isolation, characterization, and mapping of four novel polymorphic markers and an H3.3B pseudogene to chromosome 9p21-22E Aliprandis, J Harris, B Yoo, et al.
Journal of Health Care Marketing|November 5, 1991
Does greater usage of a health plan reduce satisfaction?B D Gelb, J N Gaskins, J G Hendrickson, et al.
Science (New York, N.Y.)|August 30, 1996
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiencyB D Gelb, G P Shi, H A Chapman, et al.
The Journal of Biological Chemistry|August 28, 2001
Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation propertiesF Zhao, M Satoda, J D Licht, et al.
Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.
American Journal of Medical Genetics|December 5, 2000
Char syndrome: an additional family with polythelia, a new findingR Zannolli, R Mostardini, M Matera, et al.
Genes, Chromosomes & Cancer|December 29, 1999
Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defectJ A Martignetti, B D Gelb, H Pierce, et al.
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 syndromesM Tartaglia, P D Cotter, G Zampino, et al.
Circulation|June 15, 1999
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21M Satoda, M E Pierpont, G A Diaz, 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 1q21B D Gelb, J Zhang, P D Cotter, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
Journal of Human Genetics|September 25, 1999
Isolation, characterization, and mapping of four novel polymorphic markers and an H3.3B pseudogene to chromosome 9p21-22E Aliprandis, J Harris, B Yoo, et al.
Journal of Health Care Marketing|November 5, 1991
Does greater usage of a health plan reduce satisfaction?B D Gelb, J N Gaskins, J G Hendrickson, et al.
Science (New York, N.Y.)|August 30, 1996
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiencyB D Gelb, G P Shi, H A Chapman, et al.
The Journal of Biological Chemistry|August 28, 2001
Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation propertiesF Zhao, M Satoda, J D Licht, et al.
Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.
American Journal of Medical Genetics|December 5, 2000
Char syndrome: an additional family with polythelia, a new findingR Zannolli, R Mostardini, M Matera, et al.
Genes, Chromosomes & Cancer|December 29, 1999
Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defectJ A Martignetti, B D Gelb, H Pierce, et al.
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 syndromesM Tartaglia, P D Cotter, G Zampino, et al.
Circulation|June 15, 1999
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21M Satoda, M E Pierpont, G A Diaz, 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 1q21B D Gelb, J Zhang, P D Cotter, et al.
Pageof 8