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Ana Beatriz Alvarez Perez

Showing results (1-10 of 25) with videos related to

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Jornal De Pediatria|July 31, 2017
Determining the frequency of morphological characteristics in a sample of Brazilian childrenEduardo Perrone, Thais Arbocese Zanolla, Rodrigo Ambrosio Fock, et al.
American Journal of Medical Genetics. Part A|September 7, 2021
Using Online Mendelian Inheritance in Man in low- and middle-income countriesNara Lygia de Macena Sobreira, Gabriela M Repetto, Samia A Temtamy, et al.
American Journal of Medical Genetics. Part A|May 31, 2008
Complex toe syndactyly with characteristic facial phenotype: a new syndrome?Nara Lygia Macena Sobreira, Mirlene Cecilia S P Cernach, Decio Brunoni, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndromeNara Lygia de Macena Sobreira, Décio Brunoni, Mirlene Cecília Soares Pinho Cernach, et al.
Cadernos De Saude Publica|August 10, 2010
[Use of the Internet to report congenital malformations on birth certificates at four public maternity hospitals in the city of São Paulo, Brazil]Pablo Domingos Rodrigues De Nicola, Mirlene Cecília Soares Pinho Cernach, Ana Beatriz Alvarez Perez, et al.
European Journal of Medical Genetics|January 22, 2016
Novel frameshift variant in gene SALL4 causing Okihiro syndromeLeandro Ucela Alves, Ana Beatriz Alvarez Perez, Luis Garcia Alonso, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifidaAna Beatriz Alvarez Perez, Vânia D'Almeida, Naja Vergani, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 16, 2020
TRANSLATION, CULTURAL ADAPTATION, AND EVIDENCE OF INSTRUMENT VALIDITY FOR A MORPHOLOGICAL EXAMINATION PERFORMED IN CHILDREN WITH AUTISM SPECTRUM DISORDERThais Arbocese Zanolla, Eduardo Perrone, Rodrigo Ambrosio Fock, et al.
Clinical Dysmorphology|April 5, 2008
Mandibulofacial dysostosis, acral anomalies and frontonasal dysplasia: a new form of acrofacial dysostosisNara Lygia de Macena Sobreira, Maria Tereza S Alves, Ana Beatriz Alvarez Perez, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Jornal De Pediatria|July 31, 2017
Determining the frequency of morphological characteristics in a sample of Brazilian childrenEduardo Perrone, Thais Arbocese Zanolla, Rodrigo Ambrosio Fock, et al.
American Journal of Medical Genetics. Part A|September 7, 2021
Using Online Mendelian Inheritance in Man in low- and middle-income countriesNara Lygia de Macena Sobreira, Gabriela M Repetto, Samia A Temtamy, et al.
American Journal of Medical Genetics. Part A|May 31, 2008
Complex toe syndactyly with characteristic facial phenotype: a new syndrome?Nara Lygia Macena Sobreira, Mirlene Cecilia S P Cernach, Decio Brunoni, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndromeNara Lygia de Macena Sobreira, Décio Brunoni, Mirlene Cecília Soares Pinho Cernach, et al.
Cadernos De Saude Publica|August 10, 2010
[Use of the Internet to report congenital malformations on birth certificates at four public maternity hospitals in the city of São Paulo, Brazil]Pablo Domingos Rodrigues De Nicola, Mirlene Cecília Soares Pinho Cernach, Ana Beatriz Alvarez Perez, et al.
European Journal of Medical Genetics|January 22, 2016
Novel frameshift variant in gene SALL4 causing Okihiro syndromeLeandro Ucela Alves, Ana Beatriz Alvarez Perez, Luis Garcia Alonso, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifidaAna Beatriz Alvarez Perez, Vânia D'Almeida, Naja Vergani, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 16, 2020
TRANSLATION, CULTURAL ADAPTATION, AND EVIDENCE OF INSTRUMENT VALIDITY FOR A MORPHOLOGICAL EXAMINATION PERFORMED IN CHILDREN WITH AUTISM SPECTRUM DISORDERThais Arbocese Zanolla, Eduardo Perrone, Rodrigo Ambrosio Fock, et al.
Clinical Dysmorphology|April 5, 2008
Mandibulofacial dysostosis, acral anomalies and frontonasal dysplasia: a new form of acrofacial dysostosisNara Lygia de Macena Sobreira, Maria Tereza S Alves, Ana Beatriz Alvarez Perez, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
Pageof 3