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Aesthetic Plastic Surgery
|
September 6, 2023
Treatment of Atrophy of the Labia Majora: Calcium Hydroxyapatite or Hyaluronic Acid?
Clarissa Lima Vilela, Gladstone Eustaquio de Lima Faria, Ricardo Frota Boggio
Lancet (London, England)
|
July 30, 1977
Risk of 45,X karyotype in offspring of Turner's syndrome patients
P A Otto, S Kasahara, H G Nunesmaia, et al.
Journal De Genetique Humaine
|
June 1, 1976
Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study
M Zatz, O Frota-Pessoa, J A Levy, et al.
Physical Review Letters
|
September 23, 1996
Magnetic Behavior of Fe Impurities in Tc and Re, and Its Relevance to the General Problem of the Magnetism of Fe in d-Band Metal Hosts
Kapoor, Andres, Mezei, et al.
Journal of Medical Genetics
|
April 1, 1984
Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome
A Richieri-Costa, S M Garcia da Silva, O Frota-Pessoa
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo
|
May 31, 2023
Profile of children assisted in a teaching outpatient clinic of developmental disabilities in São Paulo, Brazil
Melina Alves da Frota, Rosa Miranda Resegue, Anete Colucci, et al.
Infection and Immunity
|
August 24, 2004
The AraC family transcriptional regulator Rv1931c plays a role in the virulence of Mycobacterium tuberculosis
Cristiane C Frota, K G Papavinasasundaram, Elaine O Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 19, 2005
Frequency and phenotypic consequences of the 3199del6 CFTR mutation in French Canadians
Andrea Frota Ruchon, Shannon R Ryan, Raouf Fetni, et al.
Ciencia & Saude Coletiva
|
December 21, 2019
Health and nursing system in France
Christine Guesdon-Caltero, Nadia Cherchem, Mirna Albuquerque Frota, et al.
American Journal of Medical Genetics
|
January 1, 1981
Autosomal dominant late adult spinal muscular atrophy, type Finkel
A Richieri-Costa, A Rogatko, R Levisky, et al.
Page
of 115
Search research articles
Search
Showing results (121-130 of 1,150) with videos related to
Sort By:
Page
of 115
Aesthetic Plastic Surgery
|
September 6, 2023
Treatment of Atrophy of the Labia Majora: Calcium Hydroxyapatite or Hyaluronic Acid?
Clarissa Lima Vilela, Gladstone Eustaquio de Lima Faria, Ricardo Frota Boggio
Lancet (London, England)
|
July 30, 1977
Risk of 45,X karyotype in offspring of Turner's syndrome patients
P A Otto, S Kasahara, H G Nunesmaia, et al.
Journal De Genetique Humaine
|
June 1, 1976
Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study
M Zatz, O Frota-Pessoa, J A Levy, et al.
Physical Review Letters
|
September 23, 1996
Magnetic Behavior of Fe Impurities in Tc and Re, and Its Relevance to the General Problem of the Magnetism of Fe in d-Band Metal Hosts
Kapoor, Andres, Mezei, et al.
Journal of Medical Genetics
|
April 1, 1984
Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome
A Richieri-Costa, S M Garcia da Silva, O Frota-Pessoa
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo
|
May 31, 2023
Profile of children assisted in a teaching outpatient clinic of developmental disabilities in São Paulo, Brazil
Melina Alves da Frota, Rosa Miranda Resegue, Anete Colucci, et al.
Infection and Immunity
|
August 24, 2004
The AraC family transcriptional regulator Rv1931c plays a role in the virulence of Mycobacterium tuberculosis
Cristiane C Frota, K G Papavinasasundaram, Elaine O Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 19, 2005
Frequency and phenotypic consequences of the 3199del6 CFTR mutation in French Canadians
Andrea Frota Ruchon, Shannon R Ryan, Raouf Fetni, et al.
Ciencia & Saude Coletiva
|
December 21, 2019
Health and nursing system in France
Christine Guesdon-Caltero, Nadia Cherchem, Mirna Albuquerque Frota, et al.
American Journal of Medical Genetics
|
January 1, 1981
Autosomal dominant late adult spinal muscular atrophy, type Finkel
A Richieri-Costa, A Rogatko, R Levisky, et al.
Page
of 115