skip to main content
Idioma:
Mostrar Somente
Refinado por: assunto: Humans remover xxx: xxx remover Medical Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Molecular markers of head and neck squamous cell carcinoma: Promising signs in need of prospective evaluation
Molecular markers of head and neck squamous cell carcinoma: Promising signs in need of prospective evaluation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular markers of head and neck squamous cell carcinoma: Promising signs in need of prospective evaluation

Lothaire, Phillipe ; de Azambuja, Evandro ; Dequanter, Didier ; Lalami, Yassine ; Sotiriou, Christos ; Andry, Guy ; Castro Jr, Gilberto ; Awada, Ahmad

Head & neck, 2006-03, Vol.28 (3), p.256-269 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
2
Prenatal sonographic diagnosis of the 49,XXXXY syndrome
Prenatal sonographic diagnosis of the 49,XXXXY syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Prenatal sonographic diagnosis of the 49,XXXXY syndrome

Schluth, Caroline ; Doray, Bérénice ; Girard-Lemaire, Françoise ; Kohler, Monique ; Langer, Bruno ; Gasser, Bernard ; Lindner, Véronique ; Flori, Elisabeth

Prenatal diagnosis, 2002-12, Vol.22 (13), p.1177-1180 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

Texto completo disponível

Citações Citado por
3
Professional Characteristics and Job Satisfaction Among SGIM Members: A Comparison of Part-time and Full-time Physician Members
Professional Characteristics and Job Satisfaction Among SGIM Members: A Comparison of Part-time and Full-time Physician Members
Material Type:
Artigo 		Adicionar ao Meu Espaço

Professional Characteristics and Job Satisfaction Among SGIM Members: A Comparison of Part-time and Full-time Physician Members

Levine, Rachel B. ; Harrison, Rebecca A. ; Mechaber, Hilit F. ; Phillips, Christopher ; Gallagher, Thomas H.

Journal of general internal medicine : JGIM, 2008-08, Vol.23 (8), p.1218-1221 [Periódico revisado por pares]

New York: Springer-Verlag

Texto completo disponível

Citações Citado por
4
Cardiovascular Phenotype in Turner Syndrome—Integrating Cardiology, Genetics, and Endocrinology
Cardiovascular Phenotype in Turner Syndrome—Integrating Cardiology, Genetics, and Endocrinology
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cardiovascular Phenotype in Turner Syndrome—Integrating Cardiology, Genetics, and Endocrinology

Mortensen, Kristian H ; Andersen, Niels H ; Gravholt, Claus H

Endocrine reviews, 2012-10, Vol.33 (5), p.677-714 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

Texto completo disponível

Citações Citado por
5
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies

GRATI, Francesca R ; SIRCHIA, Silvia M ; MIOZZO, Monica ; GENTILIN, Barbara ; ROSSELLA, Franca ; RAMOSCELLI, Lisetta ; ANTONAZZO, Patrizio ; CAVALLARI, Ugo ; BULFAMANTE, Gaetano ; CETIN, Irene ; SIMONI, Giuseppe

European journal of human genetics : EJHG, 2004-04, Vol.12 (4), p.272-278 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing

Texto completo disponível

Citações Citado por
6
The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: Follow up in a 14-year-old girl
The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: Follow up in a 14-year-old girl
Material Type:
Artigo 		Adicionar ao Meu Espaço

The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: Follow up in a 14-year-old girl

Rittinger, Olaf ; Kronberger, Gabriela ; Pfeifenberger, Andrea ; Kotzot, Dieter ; Fauth, Christine

European journal of medical genetics, 2008-11, Vol.51 (6), p.573-579 [Periódico revisado por pares]

Amsterdam: Elsevier Masson SAS

Texto completo disponível

Citações Citado por
7
Frontiers in Preclinical Safety Biomarkers: MicroRNAs and Messenger RNAs
Frontiers in Preclinical Safety Biomarkers: MicroRNAs and Messenger RNAs
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frontiers in Preclinical Safety Biomarkers: MicroRNAs and Messenger RNAs

Mikaelian, Igor ; Scicchitano, Marshall ; Mendes, Odete ; Thomas, Roberta A. ; LeRoy, Bruce E.

Toxicologic pathology, 2013-01, Vol.41 (1), p.18-31 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

Texto completo disponível

Citações Citado por
8
Lack of meiotic crossovers during oogenesis in an apparent 45,X Ullrich–Turner syndrome patient with three children
Lack of meiotic crossovers during oogenesis in an apparent 45,X Ullrich–Turner syndrome patient with three children
Material Type:
Artigo 		Adicionar ao Meu Espaço

Lack of meiotic crossovers during oogenesis in an apparent 45,X Ullrich–Turner syndrome patient with three children

Houge, Gunnar ; Boman, Helge ; Lybæk, Helle ; Ness, Gro O. ; Juliusson, Petur B.

American journal of medical genetics. Part A, 2006-05, Vol.140A (10), p.1092-1097 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
9
Genes and translocations involved in POF
Genes and translocations involved in POF
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genes and translocations involved in POF

Schlessinger, David ; Herrera, Luisa ; Crisponi, Laura ; Mumm, Steven ; Percesepe, Antonio ; Pellegrini, Massimo ; Pilia, Giuseppe ; Forabosco, Antonino

American journal of medical genetics, 2002-08, Vol.111 (3), p.328-333

New York: Wiley Subscription Services, Inc., A Wiley Company

Texto completo disponível

Citações Citado por
10
Reproductive genetic counselling in non‐mosaic 47,XXY patients: implications for preimplantation or prenatal diagnosis: Case report and review
Reproductive genetic counselling in non‐mosaic 47,XXY patients: implications for preimplantation or prenatal diagnosis: Case report and review
Material Type:
Artigo 		Adicionar ao Meu Espaço

Reproductive genetic counselling in non‐mosaic 47,XXY patients: implications for preimplantation or prenatal diagnosis: Case report and review

Tachdjian, Gérard ; Frydman, Nelly ; Morichon‐Delvallez, Nicole ; Dû, Anne Le ; Fanchin, Renato ; Vekemans, Michel ; Frydman, René

Human reproduction (Oxford), 2003-02, Vol.18 (2), p.271-275 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (11)

Data de Publicação 

De até
Refinar
  1. Antes de2002  (1)
  2. 2002Até2002  (3)
  3. 2003Até2003  (1)
  4. 2004Até2006  (4)
  5. Após 2006  (5)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.