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S N Thibodeau

Showing results (61-70 of 156) with videos related to

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The American Journal of Cardiology|December 15, 1994
Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7qA Kumar, T M Olson, S N Thibodeau, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Mayo Clinic Proceedings|May 1, 1997
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significanceH M Heshmati, H Gharib, S Khosla, et al.
Hemoglobin|March 11, 1998
Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-AmericansJ D Hoyer, M J Wick, S N Thibodeau, et al.
Journal of Medical Genetics|January 1, 1992
Exclusion of calcitonin/alpha-CGRP gene defect in a family with autosomal dominant supravalvular aortic stenosisG M Pastores, V V Michels, D J Schaid, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.
Hemoglobin|November 1, 1996
Hb Cook [beta 132(H10)Lys-->Thr]: a new hemoglobin variant in a southeast Asian familyP J Hutt, V F Fairbanks, T C Griffin, et al.
Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 18, 1998
Cystic fibrosis and the phenotypic expression of autosomal dominant polycystic kidney diseaseD A O'Sullivan, V E Torres, P A Gabow, et al.
Neurogenetics|May 1, 1997
The genomic organization of human dystrobrevinH M Sadoulet-Puccio, C A Feener, D J Schaid, et al.
Pageof 16

Showing results (61-70 of 156) with videos related to

Sort By:
Pageof 16
The American Journal of Cardiology|December 15, 1994
Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7qA Kumar, T M Olson, S N Thibodeau, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Mayo Clinic Proceedings|May 1, 1997
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significanceH M Heshmati, H Gharib, S Khosla, et al.
Hemoglobin|March 11, 1998
Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-AmericansJ D Hoyer, M J Wick, S N Thibodeau, et al.
Journal of Medical Genetics|January 1, 1992
Exclusion of calcitonin/alpha-CGRP gene defect in a family with autosomal dominant supravalvular aortic stenosisG M Pastores, V V Michels, D J Schaid, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.
Hemoglobin|November 1, 1996
Hb Cook [beta 132(H10)Lys-->Thr]: a new hemoglobin variant in a southeast Asian familyP J Hutt, V F Fairbanks, T C Griffin, et al.
Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 18, 1998
Cystic fibrosis and the phenotypic expression of autosomal dominant polycystic kidney diseaseD A O'Sullivan, V E Torres, P A Gabow, et al.
Neurogenetics|May 1, 1997
The genomic organization of human dystrobrevinH M Sadoulet-Puccio, C A Feener, D J Schaid, et al.
Pageof 16