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1
Androgen insensitivity syndrome mutations in exon 3 of AR gene in patients with partial and mild forms
Androgen insensitivity syndrome mutations in exon 3 of AR gene in patients with partial and mild forms
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Artigo de Congresso 		Adicionar ao Meu Espaço

Androgen insensitivity syndrome mutations in exon 3 of AR gene in patients with partial and mild forms

C. Vretos Ester Silveira Ramos; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 179, res. P0651, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617815 ) e outros locais(Acessar)

2
NANOG expression in Ewing's sarcoma and desmoplastic small round cell tumor
NANOG expression in Ewing's sarcoma and desmoplastic small round cell tumor
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

NANOG expression in Ewing's sarcoma and desmoplastic small round cell tumor

A. F. L. Rios Luiz Gonzaga Tone; Carlos Alberto Scridelli; R. P Queiroz; Ester Silveira Ramos; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 164, res. P0584, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617809 ) e outros locais(Acessar)

3
Case report patient with ring chromosome 4
Case report patient with ring chromosome 4
Material Type:
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Case report patient with ring chromosome 4

J. Huber Ester Silveira Ramos; D. G Melo; Lúcia Regina Martelli; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 122, res. P0397, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617794 ) e outros locais(Acessar)

4
Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies
Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies
Material Type:
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Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies

M. V. M. Gomes J Huber; Rui Alberto Ferriani; Ester Silveira Ramos; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 180, res. P0656, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617820 ) e outros locais(Acessar)

5
Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms
Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms
Material Type:
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Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms

F. M. Araújo M. R Soares; M. V. M Gomes; Geraldo Duarte; C. R Marcondes; P. A Vozzi; Raysildo Barbosa Lôbo; Ester Silveira Ramos; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 251, res. P0980, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617858 ) e outros locais(Acessar)

6
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY
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Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY

Marcelo Razera Baruffi Carlos Alberto Scrideli; J. A Squire; J Karaskowa; Ester Silveira Ramos; B Heck; Luiz Gonzaga Tone; European Human Genetics Conference 2002 (2002 Strasbourg); European Meeting on Psychosocial Aspects of Genetics 2002 (2002 Strasbourg)

European Journal of Human Genetics New York v. 10, suppl. 1, p. 91 res. P0082, 2002

New York 2002

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1276462 ) e outros locais(Acessar)

7
Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly
Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly

Ester Silveira Ramos A Araújo; C. D Martinhago; Lúcia Regina Martelli; Rosana Maria dos Reis; D. G Melo; European Human Genetics Conference (2007 Nice)

European Journal of Human Genetics London v. 15, suppl. 1, p. 92, res. P0260, 2007

London 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1617770 ) e outros locais(Acessar)

8
Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers
Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers

Ester Silveira Ramos Lúcia Regina Martelli; J Karaskowa; J Huber; L. D. R Giuliani; Beatriz R Versiani; Maria Lúcia Machado; Lucimar A. F Laureano; J Squire; European Human Genetics Conference (2002 Strasbourg); European Meeting on Psychosocial Aspects of Genetics (2002 Strasbourg)

European Journal of Human Genetics London v. 10, supl. 1, p. 132, res. P0273, 2002

2002

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1294955 ) e outros locais(Acessar)

9
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development
Material Type:
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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

BHOJ, Elizabeth J ; RAMOS, Purita ; VANHOUTTEGHEM, Amandine ; DJIAN, Philippe ; ZINN, Andrew R ; BAKER, Linda A ; COST, Nicholas ; NORDENSKJÖLD, Agneta ; ELDER, Frederick F ; BLEYL, Steven B ; BOWLES, Neil E ; ARRINGTON, Cammon B ; DELHOMME, Brigitte

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.540-546 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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10
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
Material Type:
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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

Ockeloen, Charlotte W ; Willemsen, Marjolein H ; de Munnik, Sonja ; van Bon, Bregje WM ; de Leeuw, Nicole ; Verrips, Aad ; Kant, Sarina G ; Jones, Elizabeth A ; Brunner, Han G ; van Loon, Rosa LE ; Smeets, Eric EJ ; van Haelst, Mieke M ; van Haaften, Gijs ; Nordgren, Ann ; Malmgren, Helena ; Grigelioniene, Giedre ; Vermeer, Sascha ; Louro, Pedro ; Ramos, Lina ; Maal, Thomas JJ ; van Heumen, Celeste C ; Yntema, Helger G ; Carels, Carine ; Kleefstra, Tjitske

European Journal of Human Genetics, 2015-09, Vol.23 (9), p.1176-1185 [Periódico revisado por pares]

Nature Publishing Group

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