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B T Teh

Showing results (61-70 of 128) with videos related to

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The American Journal of Pathology|February 10, 2000
Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiologyE Edström, E Mahlamäki, B Nord, et al.
Journal of Medical Genetics|May 5, 1999
Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one familyB T Teh, K Linblad, B Nord, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 27, 2000
Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate familiesF K Wong, C Hagberg, A Karsten, et al.
Clinical Genetics|January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindredB T Teh, A A Sullivan, F Farnebo, et al.
Lancet (London, England)|March 22, 1997
Familial non-VHL non-papillary clear-cell renal cancerB T Teh, S Giraud, N F Sari, et al.
Human Molecular Genetics|October 1, 1994
The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumoursG Weber, E Friedman, S Grimmond, et al.
Genes, Chromosomes & Cancer|April 2, 1998
Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitutionB T Teh, E Blennow, S Giraud, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipationS Giraud, H Choplin, B T Teh, et al.
World Journal of Surgery|December 5, 1998
Evaluation of retinoblastoma and Ki-67 immunostaining as diagnostic markers of benign and malignant parathyroid diseaseF Farnebo, G Auer, L O Farnebo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomasB T Teh, F Farnebo, U Kristoffersson, et al.
Pageof 13

Showing results (61-70 of 128) with videos related to

Sort By:
Pageof 13
The American Journal of Pathology|February 10, 2000
Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiologyE Edström, E Mahlamäki, B Nord, et al.
Journal of Medical Genetics|May 5, 1999
Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one familyB T Teh, K Linblad, B Nord, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 27, 2000
Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate familiesF K Wong, C Hagberg, A Karsten, et al.
Clinical Genetics|January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindredB T Teh, A A Sullivan, F Farnebo, et al.
Lancet (London, England)|March 22, 1997
Familial non-VHL non-papillary clear-cell renal cancerB T Teh, S Giraud, N F Sari, et al.
Human Molecular Genetics|October 1, 1994
The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumoursG Weber, E Friedman, S Grimmond, et al.
Genes, Chromosomes & Cancer|April 2, 1998
Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitutionB T Teh, E Blennow, S Giraud, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipationS Giraud, H Choplin, B T Teh, et al.
World Journal of Surgery|December 5, 1998
Evaluation of retinoblastoma and Ki-67 immunostaining as diagnostic markers of benign and malignant parathyroid diseaseF Farnebo, G Auer, L O Farnebo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomasB T Teh, F Farnebo, U Kristoffersson, et al.
Pageof 13