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American Journal of Medical Genetics
|
August 8, 1997
Unsuspected mutation in a family with congenital adrenal hyperplasia
J 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 2A
G 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 Cys609Phe
J 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 familial
J 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 gene
J 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 gene
J 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 gene
S 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 region
M 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 neoplasms
J Oriola, I Halperin, C Mallofré, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
August 8, 1997
Unsuspected mutation in a family with congenital adrenal hyperplasia
J 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 2A
G 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 Cys609Phe
J 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 familial
J 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 gene
J 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 gene
J 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 gene
S 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 region
M 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 neoplasms
J Oriola, I Halperin, C Mallofré, et al.
Page
of 4