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Refinado por: Nome da Publicação: American Journal of Medical Genetics (Neuropsychiatric Genetics) remover
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11
Association of the C766T polymorphism of the low-density lipoprotein receptor-related protein gene with Alzheimer's disease
Association of the C766T polymorphism of the low-density lipoprotein receptor-related protein gene with Alzheimer's disease
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Association of the C766T polymorphism of the low-density lipoprotein receptor-related protein gene with Alzheimer's disease

Kölsch, Heike ; Ptok, Ursula ; Mohamed, Iman ; Schmitz, Sandra ; Rao, Marie Luise ; Maier, Wolfgang ; Heun, Reinhard

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-08, Vol.121B (1), p.128-130 [Periódico revisado por pares]

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

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12
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
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Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia

Canki-Klain, Nina ; Milic, Astrid ; Kovac, Biserka ; Trlaja, Anuska ; Grgicevic, Damir ; Zurak, Niko ; Fardeau, Michel ; Leturcq, France ; Kaplan, Jean-Claude ; Urtizberea, J. Andoni ; Politano, Luisa ; Piluso, Giulio ; Feingold, Josue

American journal of medical genetics, 2004-03, Vol.125A (2), p.152-156 [Periódico revisado por pares]

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

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13
Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease
Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease
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Association between the TNFα-308 A/G polymorphism and the onset-age of Alzheimer disease

Alvarez, Victoria ; Mata, Ignacio F. ; González, Pelayo ; Lahoz, Carlos H. ; Martínez, Carmen ; Peña, Joaquín ; Guisasola, Luis M. ; Coto, Eliecer

American journal of medical genetics, 2002-07, Vol.114 (5), p.574-577 [Periódico revisado por pares]

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

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14
An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease
An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease
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An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease

Rosenmann, Hanna ; Meiner, Zeev ; Kahana, Esther ; Aladjem, Zoja ; Friedman, Gideon ; Ben-Yehuda, Arie ; Grenader, Tal ; Wertman, Eli ; Abramsky, Oded

American journal of medical genetics, 2004-07, Vol.128B (1), p.123-125 [Periódico revisado por pares]

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

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15
Polymorphisms of the σ1 receptor gene in schizophrenia: An association study
Polymorphisms of the σ1 receptor gene in schizophrenia: An association study
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Polymorphisms of the σ1 receptor gene in schizophrenia: An association study

Ohmori, Osamu ; Shinkai, Takahiro ; Suzuki, Takashi ; Okano, Chie ; Kojima, Hideki ; Terao, Takeshi ; Nakamura, Jun

American journal of medical genetics, 2000-02, Vol.96 (1), p.118-122 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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16
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter
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Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter

Sarri, C. ; Gyftodimou, J. ; Avramopoulos, D. ; Grigoriadou, M. ; Pedersen, W. ; Pandelia, E. ; Pangalos, C. ; Abazis, D. ; Kitsos, G. ; Vassilopoulos, D. ; Brøndum-Nielsen, K. ; Petersen, M. B.

American journal of medical genetics, 1997-05, Vol.70 (1), p.87-94 [Periódico revisado por pares]

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

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17
Pigmentary mosaicism of the hyperpigmented type in two half‐brothers
Pigmentary mosaicism of the hyperpigmented type in two half‐brothers
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Pigmentary mosaicism of the hyperpigmented type in two half‐brothers

Horn, Denise ; Happle, Rudolf ; Neitzel, Heidemarie ; Kunze, Jürgen

American journal of medical genetics, 2002-09, Vol.112 (1), p.65-69

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

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18
Social adjustment in adult males affected with progressive muscular dystrophy
Social adjustment in adult males affected with progressive muscular dystrophy
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Social adjustment in adult males affected with progressive muscular dystrophy

Eggers, Sabine ; Zatz, Mayana

American journal of medical genetics, 1998-02, Vol.81 (1), p.4-12 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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19
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
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Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G

Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S. ; Zatz, Mayana

American journal of medical genetics, 1999-02, Vol.82 (5), p.392-398

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

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20
Frequent loss of imprinting of the H19 and IGF-II genes in ovarian tumors
Frequent loss of imprinting of the H19 and IGF-II genes in ovarian tumors
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Frequent loss of imprinting of the H19 and IGF-II genes in ovarian tumors

Kim, Hong Tae ; Choi, Bo Hwa ; Niikawa, Norio ; Lee, Tae Sung ; Chang, Sung Ik

American journal of medical genetics, 1998-12, Vol.80 (4), p.391-395

New York: John Wiley & Sons, Inc

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Deste Autor:

  1. Lauriano, V
  2. Passos-Bueno, M
  3. Frota-Pessoa, O
  4. Melo, M
  5. Eggers, S

Neste Assunto:

  1. Medical Sciences
  2. Biological And Medical Sciences
  3. Humans
  4. Genetics & Heredity
  5. Life Sciences & Biomedicine

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

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