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J Oriola

Showing results (1-10 of 36) with videos related to

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American Journal of Medical Genetics|August 8, 1997
Unsuspected mutation in a family with congenital adrenal hyperplasiaJ Oriola, C Pavia
Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
False-positive results of basal and pentagastrin-stimulated calcitonin in non-gene carriers of multiple endocrine neoplasia type 2AG Hernández, R Simó, J Oriola, et al.
Clinical Genetics|June 28, 2012
Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609PheJ Oriola, J Biarnes, C Hernandez, et al.
Journal of Endocrinological Investigation|March 9, 2002
The finding of a somaticdeletion in RET exon 15 clarified the sporadic nature of amedullary thyroid carcinoma suspected to be familialJ Oriola, I Halperin, F Rivera-Fillat, et al.
Medicina Clinica|June 11, 1999
[Genetic study of a new family with Hippel-Lindau type IIB disease]G Cuatrecasas, J Oriola, M L Granada, et al.
Clinical Chemistry|April 1, 1997
Rapid screening method for detecting mutations in the 21-hydroxylase geneJ Oriola, I Plensa, I Machuca, et al.
Clinical Genetics|May 1, 1997
Short report on DNA markers at candidate loci. Two new polymorphisms in the BRCA 1 geneJ Oriola, E Titos, A Leivas, et al.
Clinical Genetics|February 1, 1997
MspI identifies a biallelic polymorphism in the promoter region of the alpha 2A-adrenergic receptor geneS Lario, J Calls, A Cases, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1996
Polymorphisms of the human alpha 2A-adrenergic receptor gene in a Catalan population: description of a new polymorphism in the promoter regionM Bono, A Cases, J Oriola, et al.
European Journal of Cancer (Oxford, England : 1990)|November 27, 2001
Screening of selected genomic areas potentially involved in thyroid neoplasmsJ Oriola, I Halperin, C Mallofré, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|August 8, 1997
Unsuspected mutation in a family with congenital adrenal hyperplasiaJ Oriola, C Pavia
Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
False-positive results of basal and pentagastrin-stimulated calcitonin in non-gene carriers of multiple endocrine neoplasia type 2AG Hernández, R Simó, J Oriola, et al.
Clinical Genetics|June 28, 2012
Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609PheJ Oriola, J Biarnes, C Hernandez, et al.
Journal of Endocrinological Investigation|March 9, 2002
The finding of a somaticdeletion in RET exon 15 clarified the sporadic nature of amedullary thyroid carcinoma suspected to be familialJ Oriola, I Halperin, F Rivera-Fillat, et al.
Medicina Clinica|June 11, 1999
[Genetic study of a new family with Hippel-Lindau type IIB disease]G Cuatrecasas, J Oriola, M L Granada, et al.
Clinical Chemistry|April 1, 1997
Rapid screening method for detecting mutations in the 21-hydroxylase geneJ Oriola, I Plensa, I Machuca, et al.
Clinical Genetics|May 1, 1997
Short report on DNA markers at candidate loci. Two new polymorphisms in the BRCA 1 geneJ Oriola, E Titos, A Leivas, et al.
Clinical Genetics|February 1, 1997
MspI identifies a biallelic polymorphism in the promoter region of the alpha 2A-adrenergic receptor geneS Lario, J Calls, A Cases, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|August 1, 1996
Polymorphisms of the human alpha 2A-adrenergic receptor gene in a Catalan population: description of a new polymorphism in the promoter regionM Bono, A Cases, J Oriola, et al.
European Journal of Cancer (Oxford, England : 1990)|November 27, 2001
Screening of selected genomic areas potentially involved in thyroid neoplasmsJ Oriola, I Halperin, C Mallofré, et al.
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