Go to:
Logótipo
You are here: Start > Publications > View > Disease: Adrenal hyperplasia
Today is sunday
BIN@Porto 2024
Publication

Disease: Adrenal hyperplasia

Title
Disease: Adrenal hyperplasia
Type
Another Publication in an International Scientific Journal
Year
2010
Authors
Carvalho, B
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Carvalho, Davide
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page Without ORCID
barros, a
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
carvalho, f
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Journal
Title: Human GeneticsImported from Authenticus Search for Journal Publications
Vol. 127
Final page: 482
ISSN: 0340-6717
Publisher: Springer Nature
Indexing
Publicação em Scopus Scopus - 0 Citations
Other information
Authenticus ID: P-008-4V3
Language: English
Type (Professor's evaluation): Scientific
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same authors

Novel human pathological mutations. Gene symbol: CYP21A2. Disease: adrenal hyperplasia. (2010)
Article in International Scientific Journal
Carvalho, B; Marques, CJ; Carvalho, Davide; barros, a; carvalho, f
Mutational Characterization of Steroid 21-Hydroxylase Gene in Portuguese patients with Congenital Adrenal Hyperplasia (2010)
Article in International Scientific Journal
Marques, CJ; Pignatelli, D; Carvalho, B; Barcelo, J; Almeida, AC; Fernandes, S; Witchel, SF; sousa, m; Oliveira, MJ; Freitas, P; Fontoura M; Carvalho, Davide; barros, a; carvalho, f
Comprehensive Genetic Analysis and Structural Characterization of CYP21A2 Mutations in CAH Patients (2012)
Article in International Scientific Journal
Carvalho, B; Pereira, M; Marques, CJ; Carvalho, Davide; Leao, M; João Paulo Oliveira; barros, a; carvalho, f

Of the same journal

Nature meets nurture: molecular genetics of gastric cancer (2009)
Another Publication in an International Scientific Journal
Milne, AN; Carneiro F; O'Morain, C; Offerhaus, GJA
LINKAGE ANALYSES OF HUMAN PEPTIDASE-C (PEPC), HUMAN FACTOR-H (HF), AND COAGULATION FACTOR-XIIIB (F13B) (1989)
Another Publication in an International Scientific Journal
KOMPF, J; LUCKENBACH, C; KLOOR, D; KRCZAL, D; AMORIM, A; RITTER, H
HUMAN PHOSPHOGLYCOLATE PHOSPHATASE (PGP) EC 3.1.3.18 - LINKAGE ANALYSIS (1980)
Another Publication in an International Scientific Journal
SIEBERT, G; AMORIM, A; KOMPF, J
HAPLOTYPE ANALYSIS OF COMMON TRANSTHYRETIN MUTATIONS (1995)
Another Publication in an International Scientific Journal
ALMEIDA, MR; AOYAMAOISHI, N; SAKAKI, Y; HOLMGREN, G; ULF, D; FERLINI, A; SALVI, F; MUNARQUES, M; BENSON, MD; SKINNER, M; COSTA, PP; SARAIVA, MJ
GENETIC-POLYMORPHISM OF HUMAN PEPTIDASE-C, PEPC (EC3411) - FORMAL GENETIC AND POPULATION-DATA (1989)
Another Publication in an International Scientific Journal
KOMPF, J; PRATA, MJ; AMORIM, A

See all (41)

Recommend this page Top
Copyright 1996-2024 © Faculdade de Engenharia da Universidade do Porto  I Terms and Conditions  I Accessibility  I Index A-Z  I Guest Book
Page generated on: 2024-09-29 at 20:45:17 | Acceptable Use Policy | Data Protection Policy | Complaint Portal