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Refinado por: Nome da Publicação: Journal Of Medical Genetics remover
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1
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Artigo
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Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families

Maria Rita Passos-Bueno I Richard; Mariz Vainzof; F Fougerousse; J Weissenbach; O Broux; D Cohen; J Akiyama; Suely Kazue Nagahashi Marie; A. A Carvalho; L Guilherme

London v.30, n.5 , p.385-7, 1993 Journal of Medical Genetics

London 1993

Item não circula. Consulte sua biblioteca.(Acessar)

2
Material Type:
Artigo
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Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families

Maria Rita Passos-Bueno I Richard; M Vainzof; F Fougerousse; J Weissenbach; O Broux; D Cohen; J Akiyama; Suely Kazue Nagahashi Marie; A. A Carvalho; L Guilherme

London v.30, n.5 , p.385-7, 1993 Journal of Medical Genetics

London 1993

Item não circula. Consulte sua biblioteca.(Acessar)

3
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients
Material Type:
Artigo
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Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients

Koyanagi, Yoshito ; Akiyama, Masato ; Nishiguchi, Koji M ; Momozawa, Yukihide ; Kamatani, Yoichiro ; Takata, Sadaaki ; Inai, Chihiro ; Iwasaki, Yusuke ; Kumano, Mikako ; Murakami, Yusuke ; Omodaka, Kazuko ; Abe, Toshiaki ; Komori, Shiori ; Gao, Dan ; Hirakata, Toshiaki ; Kurata, Kentaro ; Hosono, Katsuhiro ; Ueno, Shinji ; Hotta, Yoshihiro ; Murakami, Akira ; Terasaki, Hiroko ; Wada, Yuko ; Nakazawa, Toru ; Ishibashi, Tatsuro ; Ikeda, Yasuhiro ; Kubo, Michiaki ; Sonoda, Koh-Hei

Journal of medical genetics, 2019-10, Vol.56 (10), p.662-670 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

Texto completo disponível

4
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
Material Type:
Artigo
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Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases

Goto, Kensuke ; Koyanagi, Yoshito ; Akiyama, Masato ; Murakami, Yusuke ; Fukushima, Masatoshi ; Fujiwara, Kohta ; Iijima, Hanae ; Yamaguchi, Mitsuyo ; Endo, Mikiko ; Hashimoto, Kazuki ; Ishizu, Masataka ; Hirakata, Toshiaki ; Mizobuchi, Kei ; Takayama, Masakazu ; Ota, Junya ; Sajiki, Ai Fujita ; Kominami, Taro ; Ushida, Hiroaki ; Fujita, Kosuke ; Kaneko, Hiroki ; Ueno, Shinji ; Hayashi, Takaaki ; Terao, Chikashi ; Hotta, Yoshihiro ; Murakami, Akira ; Kuniyoshi, Kazuki ; Kusaka, Shunji ; Wada, Yuko ; Abe, Toshiaki ; Nakazawa, Toru ; Ikeda, Yasuhiro ; Momozawa, Yukihide ; Sonoda, Koh-Hei ; Nishiguchi, Koji M

Journal of medical genetics, 2024-03, p.jmg-2023-109750 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

5
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families
Material Type:
Artigo
Adicionar ao Meu Espaço

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families

Passos-Bueno, M R ; Richard, I ; Vainzof, M ; Fougerousse, F ; Weissenbach, J ; Broux, O ; Cohen, D ; Akiyama, J ; Marie, S K ; Carvalho, A A

Journal of medical genetics, 1993-05, Vol.30 (5), p.385-387 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

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Deste Autor:

  1. Vainzof, M
  2. Marie, S
  3. Passos-Bueno, M
  4. Richard, I
  5. Guilherme, L

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