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American Journal of Medical Genetics
|
April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25
F Gurrieri, P Prinos, D Tackels, et al.
American Journal of Medical Genetics
|
July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients
M Grasso, F Faravelli, C Lo Nigro, et al.
Hormone Research
|
May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
L Garavelli, P Cerruti-Mainardi, R Virdis, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
March 3, 2023
Patient-nurse ratio as an index related to healthcare-associated infections: a surveillance study
Daniela de la Rosa-Zamboni, Miroslava I Carrasco-González, Norma de Blas-Barrientos, et al.
Gut
|
June 16, 1999
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis
M P de Leon, M Pedroni, P Benatti, et al.
Journal of Medical Genetics
|
February 27, 2004
A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability
O Caluseriu, C Di Gregorio, E Lucci-Cordisco, et al.
Thrombosis and Haemostasis
|
May 11, 1999
Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration
A M Gori, G Pepe, M Attanasio, et al.
Histology and Histopathology
|
March 22, 2003
Altered Cx43 expression during myocardial adaptation to acute and chronic volume overloading
L Formigli, L Ibba-Manneschi, A M Perna, et al.
American Journal of Medical Genetics
|
September 20, 2000
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome
M Zollino, C Di Stefano, G Zampino, et al.
Human Genetics
|
July 11, 2002
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients
A M Slavotinek, C Searby, L Al-Gazali, et al.
Page
of 63
Search research articles
Search
Showing results (591-600 of 628) with videos related to
Sort By:
Page
of 63
American Journal of Medical Genetics
|
April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25
F Gurrieri, P Prinos, D Tackels, et al.
American Journal of Medical Genetics
|
July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients
M Grasso, F Faravelli, C Lo Nigro, et al.
Hormone Research
|
May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
L Garavelli, P Cerruti-Mainardi, R Virdis, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
March 3, 2023
Patient-nurse ratio as an index related to healthcare-associated infections: a surveillance study
Daniela de la Rosa-Zamboni, Miroslava I Carrasco-González, Norma de Blas-Barrientos, et al.
Gut
|
June 16, 1999
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis
M P de Leon, M Pedroni, P Benatti, et al.
Journal of Medical Genetics
|
February 27, 2004
A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability
O Caluseriu, C Di Gregorio, E Lucci-Cordisco, et al.
Thrombosis and Haemostasis
|
May 11, 1999
Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration
A M Gori, G Pepe, M Attanasio, et al.
Histology and Histopathology
|
March 22, 2003
Altered Cx43 expression during myocardial adaptation to acute and chronic volume overloading
L Formigli, L Ibba-Manneschi, A M Perna, et al.
American Journal of Medical Genetics
|
September 20, 2000
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome
M Zollino, C Di Stefano, G Zampino, et al.
Human Genetics
|
July 11, 2002
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients
A M Slavotinek, C Searby, L Al-Gazali, et al.
Page
of 63