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I Cordeiro

Showing results (1-10 of 28) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in PortugalH Santos, I Cordeiro, L Nunes
Annales De Genetique|January 1, 1986
Congenital absence of the tibiae and thumbs with polydactyly. A rare genetic disease (Werner's syndrome)I Cordeiro, H Santos, P Maroteaux
American Journal of Medical Genetics|December 1, 1989
Aplasia cutis congenita associated with congenital heart defect, not a coincidence?H Santos, I Cordeiro, I Menezes
Clinical Dysmorphology|May 13, 1999
Robinow syndrome in monozygotic twins with normal statureJ M Saraiva, I Cordeiro, H G Santos
Acta Reumatologica Portuguesa|May 10, 2014
Pharmacology of biosimilar candidate drugs in rheumatology: a literature reviewF Araújo, I Cordeiro, F Teixeira, et al.
Pediatric Dermatology|December 13, 2023
Unilateral segmental presentation and a novel EPHB4 gene variant in capillary malformation-arteriovenous malformation type 2C Valente, M B Caldeira, B Duarte, et al.
Human Reproduction (Oxford, England)|April 1, 1993
Fractured zona oocytes in in-vitro fertilization cycles stimulated with gonadotrophin-releasing hormone analogue and human menopausal gonadotrophinI Cordeiro, C Calhaz-Jorge, F Leal, et al.
Actas Dermo-Sifiliograficas|February 5, 2023
Van der Woude Syndrome and Alopecia Areata: More Than a Fortuitous Association?A L João, N Cunha, A I Cordeiro, et al.
Acta Medica Portuguesa|April 1, 1984
[Surface markers in B-cell neoplastic processes. I. Neoplasms with low density of surface immunoglobulin]I Cordeiro, C M Novo, V H Soares, et al.
Revista De Neurologia|March 28, 2008
[Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations]P C Janeiro, M S Cunha, I Cordeiro, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in PortugalH Santos, I Cordeiro, L Nunes
Annales De Genetique|January 1, 1986
Congenital absence of the tibiae and thumbs with polydactyly. A rare genetic disease (Werner's syndrome)I Cordeiro, H Santos, P Maroteaux
American Journal of Medical Genetics|December 1, 1989
Aplasia cutis congenita associated with congenital heart defect, not a coincidence?H Santos, I Cordeiro, I Menezes
Clinical Dysmorphology|May 13, 1999
Robinow syndrome in monozygotic twins with normal statureJ M Saraiva, I Cordeiro, H G Santos
Acta Reumatologica Portuguesa|May 10, 2014
Pharmacology of biosimilar candidate drugs in rheumatology: a literature reviewF Araújo, I Cordeiro, F Teixeira, et al.
Pediatric Dermatology|December 13, 2023
Unilateral segmental presentation and a novel EPHB4 gene variant in capillary malformation-arteriovenous malformation type 2C Valente, M B Caldeira, B Duarte, et al.
Human Reproduction (Oxford, England)|April 1, 1993
Fractured zona oocytes in in-vitro fertilization cycles stimulated with gonadotrophin-releasing hormone analogue and human menopausal gonadotrophinI Cordeiro, C Calhaz-Jorge, F Leal, et al.
Actas Dermo-Sifiliograficas|February 5, 2023
Van der Woude Syndrome and Alopecia Areata: More Than a Fortuitous Association?A L João, N Cunha, A I Cordeiro, et al.
Acta Medica Portuguesa|April 1, 1984
[Surface markers in B-cell neoplastic processes. I. Neoplasms with low density of surface immunoglobulin]I Cordeiro, C M Novo, V H Soares, et al.
Revista De Neurologia|March 28, 2008
[Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations]P C Janeiro, M S Cunha, I Cordeiro, et al.
Pageof 3