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Cell
|
December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
American Journal of Medical Genetics
|
November 11, 1996
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats
M Gennarelli, G Novelli, F Andreasi Bassi, et al.
Neurology
|
October 1, 1992
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat
T Ashizawa, J R Dubel, P W Dunne, et al.
Diabetes
|
September 2, 2000
The K121Q variant of the human PC-1 gene is not associated with insulin resistance or type 2 diabetes among Danish Caucasians
S K Rasmussen, S A Urhammer, A Pizzuti, et al.
Nature
|
May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosome
G Borsani, R Tonlorenzi, M C Simmler, et al.
Clinical and Experimental Medicine
|
December 1, 2012
Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata
G Conteduca, A Rossi, F Megiorni, et al.
Human Molecular Genetics
|
July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
A Pizzuti, F Amati, G Calabrese, et al.
Diabetes
|
July 27, 2001
A cluster of three single nucleotide polymorphisms in the 3'-untranslated region of human glycoprotein PC-1 gene stabilizes PC-1 mRNA and is associated with increased PC-1 protein content and insulin resistance-related abnormalities
L Frittitta, T Ercolino, M Bozzali, et al.
European Review for Medical and Pharmacological Sciences
|
June 28, 2018
Androgen insensitivity syndrome
C Gulía, S Baldassarra, A Zangari, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 13, 1999
Screening of thyrotropin receptor mutations by fine-needle aspiration biopsy in autonomous functioning thyroid nodules in multinodular goiters
V Tassi, A Di Cerbo, A Porcellini, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Cell
|
December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
American Journal of Medical Genetics
|
November 11, 1996
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats
M Gennarelli, G Novelli, F Andreasi Bassi, et al.
Neurology
|
October 1, 1992
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat
T Ashizawa, J R Dubel, P W Dunne, et al.
Diabetes
|
September 2, 2000
The K121Q variant of the human PC-1 gene is not associated with insulin resistance or type 2 diabetes among Danish Caucasians
S K Rasmussen, S A Urhammer, A Pizzuti, et al.
Nature
|
May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosome
G Borsani, R Tonlorenzi, M C Simmler, et al.
Clinical and Experimental Medicine
|
December 1, 2012
Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata
G Conteduca, A Rossi, F Megiorni, et al.
Human Molecular Genetics
|
July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
A Pizzuti, F Amati, G Calabrese, et al.
Diabetes
|
July 27, 2001
A cluster of three single nucleotide polymorphisms in the 3'-untranslated region of human glycoprotein PC-1 gene stabilizes PC-1 mRNA and is associated with increased PC-1 protein content and insulin resistance-related abnormalities
L Frittitta, T Ercolino, M Bozzali, et al.
European Review for Medical and Pharmacological Sciences
|
June 28, 2018
Androgen insensitivity syndrome
C Gulía, S Baldassarra, A Zangari, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 13, 1999
Screening of thyrotropin receptor mutations by fine-needle aspiration biopsy in autonomous functioning thyroid nodules in multinodular goiters
V Tassi, A Di Cerbo, A Porcellini, et al.
Page
of 12