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Genetics and Molecular Research : GMR
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July 19, 2014
Case report. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation
C R Quaio, Y K Koda, D R Bertola, et al.
Journal of the American Veterinary Medical Association
|
February 1, 1993
Clinical manifestations of leukocyte adhesion deficiency in cattle: 14 cases (1977-1991)
R O Gilbert, W C Rebhun, C A Kim, et al.
Pediatric Dermatology
|
July 8, 2000
AEC syndrome and CHAND syndrome: further evidence of clinical overlapping in the ectodermal dysplasias
D R Bertola, C A Kim, S M Sugayama, et al.
American Journal of Medical Genetics
|
July 31, 1995
Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q
C P Koiffmann, C H Gonzalez, A M Vianna-Morgante, et al.
Journal of Pediatric Urology
|
November 24, 2016
Lower urinary tract symptoms in children and adolescents with Williams-Beuren syndrome
Z M Sammour, J de Bessa, M Hisano, et al.
Lupus
|
February 2, 2011
Penile anthropometry in systemic lupus erythematosus patients
A P Vecchi, E F Borba, E Bonfá, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
September 23, 2003
High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups
A C Pereira, R F R Corrêa, G F Mota, et al.
Arquivos Brasileiros De Cardiologia
|
November 18, 2000
Cardiac findings in 31 patients with Noonan's syndrome
D R Bertola, C A Kim, S M Sugayama, et al.
Clinical and Experimental Dermatology
|
October 22, 2009
Angiokeratoma: a cutaneous marker of Fabry's disease
L M J Albano, C Rivitti, D R Bertola, et al.
The EMBO Journal
|
August 3, 2001
Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression
C A Kim, M L Phillips, W Kim, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Genetics and Molecular Research : GMR
|
July 19, 2014
Case report. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation
C R Quaio, Y K Koda, D R Bertola, et al.
Journal of the American Veterinary Medical Association
|
February 1, 1993
Clinical manifestations of leukocyte adhesion deficiency in cattle: 14 cases (1977-1991)
R O Gilbert, W C Rebhun, C A Kim, et al.
Pediatric Dermatology
|
July 8, 2000
AEC syndrome and CHAND syndrome: further evidence of clinical overlapping in the ectodermal dysplasias
D R Bertola, C A Kim, S M Sugayama, et al.
American Journal of Medical Genetics
|
July 31, 1995
Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q
C P Koiffmann, C H Gonzalez, A M Vianna-Morgante, et al.
Journal of Pediatric Urology
|
November 24, 2016
Lower urinary tract symptoms in children and adolescents with Williams-Beuren syndrome
Z M Sammour, J de Bessa, M Hisano, et al.
Lupus
|
February 2, 2011
Penile anthropometry in systemic lupus erythematosus patients
A P Vecchi, E F Borba, E Bonfá, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
September 23, 2003
High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups
A C Pereira, R F R Corrêa, G F Mota, et al.
Arquivos Brasileiros De Cardiologia
|
November 18, 2000
Cardiac findings in 31 patients with Noonan's syndrome
D R Bertola, C A Kim, S M Sugayama, et al.
Clinical and Experimental Dermatology
|
October 22, 2009
Angiokeratoma: a cutaneous marker of Fabry's disease
L M J Albano, C Rivitti, D R Bertola, et al.
The EMBO Journal
|
August 3, 2001
Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression
C A Kim, M L Phillips, W Kim, et al.
Page
of 6