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1
Linkage studies of bipolar disorder with chromosome 18 markers
Linkage studies of bipolar disorder with chromosome 18 markers
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage studies of bipolar disorder with chromosome 18 markers

Tim Bowen G Kirov; M Gill; G Spurlock; Homero Pinto Vallada Filho; R. M Murray; Peter McGuffin; D. A Collier; M. J Owen; N Craddock

American Journal of Medical Genetics (Neuropsychiatric Genetics) v. 88, n. 5, p. 503-509, 1999

New York 1999

Item não circula. Consulte sua biblioteca.(Acessar)

2
Linkage studies of bipolar disorder with chromosome 18 markers
Linkage studies of bipolar disorder with chromosome 18 markers
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage studies of bipolar disorder with chromosome 18 markers

Tim Bowen G Kirov; M Gill; G Spurlock; Homero Pinto Vallada Filho; R. M Murray; Peter McGuffin; D. A Collier; M. J Owen; N Craddock

American Journal of Medical Genetics (Neuropsychiatric Genetics) v. 88, n. 5, p. 503-509, 1999

New York 1999

Item não circula. Consulte sua biblioteca.(Acessar)

3
Autosome search for schizophrenia susceptibility genes in multiply affected families
Autosome search for schizophrenia susceptibility genes in multiply affected families
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Autosome search for schizophrenia susceptibility genes in multiply affected families

M. I. Rees I Fenton; N. M Williams; P Holmans; N Norton; A Cardno; P Asherson; G Spurlock; Eric Roberts; E Parfitt; R Mant; Homero Pinto Vallada Filho; E Dawson; M. W Li; D. A Collier; J. F Powell; S Nanko; M Gill; Peter McGuffin; Michael J Owen

Molecular Psychiatry v. 4, n. 4, p. 353-359, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 1999 303 )(Acessar)

4
Autosome search for schizophrenia susceptibility genes in multiply affected families
Autosome search for schizophrenia susceptibility genes in multiply affected families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosome search for schizophrenia susceptibility genes in multiply affected families

M. I. Rees I Fenton; N. M Williams; P Holmans; N Norton; A Cardno; P Asherson; G Spurlock; Eric Roberts; E Parfitt; R Mant; Homero Pinto Vallada Filho; E Dawson; M. W Li; D. A Collier; J. F Powell; S Nanko; M Gill; Peter McGuffin; Michael J Owen

Molecular Psychiatry v. 4, n. 4, p. 353-359, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 1999 303 )(Acessar)

5
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
Material Type:
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SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

Spurlock, G ; Bennett, E ; Chuzhanova, N ; Thomas, N ; Jim, H-Ping ; Side, L ; Davies, S ; Haan, E ; Kerr, B ; Huson, S M ; Upadhyaya, M

Journal of medical genetics, 2009-07, Vol.46 (7), p.431-437 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)
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Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)

Upadhyaya, M ; Kluwe, Lan ; Spurlock, G ; Monem, Bisma ; Majounie, E ; Mantripragada, K ; Ruggieri, Martino ; Chuzhanova, N ; Evans, D.G ; Ferner, R ; Thomas, N ; Guha, A ; Mautner, V

Human mutation, 2008, Vol.29 (1), p.74-82 [Periódico revisado por pares]

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

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7
Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia
Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia
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Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia

WILLIAMS, N. M ; PREECE, A ; SPURLOCK, G ; NORTON, N ; WILLIAMS, H. J ; ZAMMIT, S ; O'DONOVAN, M. C ; OWEN, M. J

Molecular psychiatry, 2003-05, Vol.8 (5), p.485-487 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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8
A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere
A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere
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A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere

Thomas, N S T ; Wiseman, K ; Spurlock, G ; MacDonald, M ; Üstek, D ; Upadhyaya, M

Journal of medical genetics, 2007-03, Vol.44 (3), p.215-218 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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9
Identification of five novel SPRED1 germline mutations in Legius syndrome
Identification of five novel SPRED1 germline mutations in Legius syndrome
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Identification of five novel SPRED1 germline mutations in Legius syndrome

Laycock-van Spyk, S ; Jim, HP ; Thomas, L ; Spurlock, G ; Fares, L ; Palmer-Smith, S ; Kini, U ; Saggar, A ; Patton, M ; Mautner, V ; Pilz, DT ; Upadhyaya, M

Clinical genetics, 2011-07, Vol.80 (1), p.93-96 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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10
A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter
A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter
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A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter

SPURLOCK, G ; HEILS, A ; LESCH, K. P ; OWEN, M. J ; HOLMANS, P ; WILLIAMS, J ; D'SOUZA, U. M ; CARDNO, A ; MURPHY, K. C ; JONES, L ; BUCKLAND, P. R ; MCGUFFIN, P

Molecular psychiatry, 1998, Vol.3 (1), p.42-49 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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Deste Autor:

  1. Owen, M
  2. Gill, M
  3. Collier, D
  4. Spurlock, G
  5. McGuffin, P

Neste Assunto:

  1. Science & Technology
  2. Physics
  3. Life Sciences & Biomedicine
  4. Naturvetenskap
  5. Natural Sciences

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

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