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Refinado por: Nome da Publicação: American Journal Of Medical Genetics remover
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1
Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2
Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2
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Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2

Wagner F Gattaz Ralf Frieboes; Hans W Moises; Liu Yang; Tao Li; Xieche Liu; Peter Vetter; Fabio Macciardi; Hai G Hwu; Fritz Henn

American Journal of Medical Genetics Salt Lake City v. 105, n. 3,p. 246-249, 8 abr 2001

Salt Lake City 2001

Item não circula. Consulte sua biblioteca.(Acessar)

2
Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2
Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2
Material Type:
Artigo 		Adicionar ao Meu Espaço

Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2

Wagner F Gattaz Ralf Frieboes; Hans W Moises; Liu Yang; Tao Li; Xieche Liu; Peter Vetter; Fabio Macciardi; Hai G Hwu; Fritz Henn

American Journal of Medical Genetics Salt Lake City v. 105, n. 3,p. 246-249, 8 abr 2001

Salt Lake City 2001

Item não circula. Consulte sua biblioteca.(Acessar)

3
Maternally inherited nonsyndromic hearing loss
Maternally inherited nonsyndromic hearing loss
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Maternally inherited nonsyndromic hearing loss

Friedman, Rick A. ; Bykhovskaya, Yelena ; Sue, Carolyn M. ; DiMauro, Salvatore ; Bradley, Robert ; Fallis-Cunningham, Rebecca ; Paradies, Nancy ; Pensak, Myles L. ; Smith, Richard J. ; Groden, Joanna ; Li, Xiaoyan C. ; Fischel-Ghodsian, Nathan

American journal of medical genetics, 1999-06, Vol.84 (4), p.369-372 [Periódico revisado por pares]

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

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4
A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads
A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads
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A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads

Lu, Yong ; Guo, Chenhong ; Liu, Qiji ; Zhang, Xiyu ; Cheng, Lin ; Li, Jiangxia ; Chen, Bingxi ; Gao, Guimin ; Zhou, Haibin ; Guo, Yishou ; Li, Yefu ; Gong, Yaoqin

American journal of medical genetics, 2003-07, Vol.120A (3), p.345-349 [Periódico revisado por pares]

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

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5
Inherited translocation t(4;5) discovered on prenatal diagnosis
Inherited translocation t(4;5) discovered on prenatal diagnosis
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Inherited translocation t(4;5) discovered on prenatal diagnosis

Nien-hu, Sun ; Fon-yen, Wang ; Jin-xia, Li ; Xian-ting, Zhou ; Shun, Tang Huo ; Omenn, Gilbert S. ; Opitz, John M.

American journal of medical genetics, 1981, Vol.8 (3), p.299-302 [Periódico revisado por pares]

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

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6
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation
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Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

Wang, Qiuju ; Li, Roughua ; Zhao, Hui ; Peters, Jennifer L. ; Liu, Qiong ; Yang, Li ; Han, Dongyi ; Greinwald Jr, John H. ; Young, Wie-Yen ; Guan, Min-Xin

American journal of medical genetics, 2005-02, Vol.133A (1), p.27-30 [Periódico revisado por pares]

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

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7
102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern han chinese populations: Lack of association
102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern han chinese populations: Lack of association
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102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern han chinese populations: Lack of association

Zhang, Xian-Ning ; Jiang, San-Duo ; He, Xin-Hui ; Zhang, Li-Na

American journal of medical genetics, 2004-04, Vol.126B (1), p.16-18 [Periódico revisado por pares]

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

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8
Mutations in CYP11B1 gene: Phenotype-genotype correlations
Mutations in CYP11B1 gene: Phenotype-genotype correlations
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Mutations in CYP11B1 gene: Phenotype-genotype correlations

Zhu, Yuan-Shan ; Cordero, Juan J. ; Can, Selcuk ; Cai, Li-Qun ; You, Xueke ; Herrera, Cecilia ; DeFillo-Ricart, Mariano ; Shackleton, Cedric ; Imperato-McGinley, Julianne

American journal of medical genetics, 2003-10, Vol.122A (3), p.193-200 [Periódico revisado por pares]

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

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9
Elevated rates of severe neural tube defects in a high‐prevalence area in Northern China
Elevated rates of severe neural tube defects in a high‐prevalence area in Northern China
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Elevated rates of severe neural tube defects in a high‐prevalence area in Northern China

Moore, Cynthia A. ; Li, Song ; Li, Zhu ; Hong, Shi‐xin ; Gu, Hai‐qin ; Berry, R. J. ; Mulinare, Joseph ; Erickson, J. David

American journal of medical genetics, 1997-12, Vol.73 (2), p.113-118 [Periódico revisado por pares]

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

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10
Association analysis of polymorphisms in the DRD4 gene and heroin abuse in Chinese subjects
Association analysis of polymorphisms in the DRD4 gene and heroin abuse in Chinese subjects
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Association analysis of polymorphisms in the DRD4 gene and heroin abuse in Chinese subjects

Li, Tao ; Zhu, Zuo-Hong ; Liu, Xiehe ; Hu, Xun ; Zhao, Jinghua ; Sham, Pak C. ; Collier, David A.

American journal of medical genetics, 2000-10, Vol.96 (5), p.616-621 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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Deste Autor:

  1. Henn, F
  2. Macciardi, F
  3. Frieboes, R
  4. Vetter, P
  5. Li, T

Neste Assunto:

  1. Humans
  2. Genetics & Heredity
  3. Life Sciences & Biomedicine
  4. Science & Technology
  5. Female

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

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