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José Cidade Rodrigues

Observed names: J C Rodrigues, J. Cidade Rodrigues, Rodrigues, José Cidade
Observed institution: Hospital Maria Pia
OpenAlex ID: A5113769201
Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome
1998 · R.A. Veitia, M. Nunes, et al. · The American Journal of Human Genetics · 71
CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions
2006 · Ana Friães, Ana Toste Rêgo, et al. · Molecular Genetics and Metabolism · 63
Congenital adrenal hyperplasia in paediatric age molecular analysis of the CYP21A2 gene and implications for genetic counselling
2019 · S. Gomes, João Alfredo de Souza Silva, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Espectro de alterações moleculares detetadas no gene CYP21A2 associadas a deficiência em 21 hidroxilase
2018 · Susana Gomes, Iris Pereira‐Caetano, et al.
Congenital adrenal hyperplasia in paediatric age: molecular analysis of the CYP21A2 gene and implications for genetic counselling
2018 · S Gomes, J Silva, et al.
Estudos preliminares para a localização do gene da granulina de granulovírus de Erinnyis ello.
2002 · Ronaldo Fiorilo dos Santos, W. Sihler, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Works count: 7
Citation count: 134
H-index: 2
I10-index: 2
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