BRUETON, G R : rechercher sur Z-Library

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51

Size class structure of three commonly traded bulbs at Faraday (Johannesburg) umuthi market: Implications for sustainability

V.J. Brueton, V.L. Williams, E.T.F. Witkowski

Journal:

South African Journal of Botany

Année:

2008

Langue:

english

Fichier:

PDF, 81 KB

english, 2008

52

Recurrent abdominal pain and Helicobacter pylori in a community-based sample of London children

JM O'Donohoe, PB Sullivan, R Scott, T Rogers, MJ Brueton, D Barltrop

Journal:

Acta Paediatrica

Année:

1996

Langue:

english

Fichier:

PDF, 354 KB

english, 1996

53

A Study of Genetic Markers in a Family with Polyendocrine Disease

M. J. Brueton, H. M. Chapel, L. P. Mackintosh

Journal:

Tissue Antigens

Année:

1980

Langue:

english

Fichier:

PDF, 117 KB

english, 1980

54

A comparison of endoscopic and capsule small intestinal biopsy techniques in children with upper gastrointestinal disorders

MA ELTUMI, PS ONG, ND FRANCIS, MJ BRUETON

Journal:

Journal of Paediatrics and Child Health

Année:

1996

Langue:

english

Fichier:

PDF, 192 KB

english, 1996

55

The Effects Of Cisapride On Gastroesophageal Reflux In Children With And Without Neurological Disorders

M. J. Brueton, G. S. Clarke, B. K. Sandhu

Journal:

Developmental Medicine & Child Neurology

Année:

1990

Langue:

english

Fichier:

PDF, 289 KB

english, 1990

56

Meningococcal antigen in diagnosis and treatment of group A meningococcal infections

H.C. Whittle, B.M. Greenwood, N.McD. Davidson, A. Tomkins, P. Tugwell, D.A. Warrell, A. Zalin, A.D.M. Bryceson, E.H.O. Parry, M. Brueton, M. Duggan, J.M.V. Oomen, A.D. Rajkovic

Journal:

The American Journal of Medicine

Année:

1975

Langue:

english

Fichier:

PDF, 597 KB

english, 1975

57

Sensorineural deafness, enamel abnormalities and nail abnormalities: a case report of Heimler syndrome in identical twin girls

K.R. Ong, S. Visram, S. McKaig, L.A. Brueton

Journal:

European Journal of Medical Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 340 KB

english, 2006

58

Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood

J. Vogt, S. Hill, L. Brueton

Journal:

European Journal of Medical Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 146 KB

english, 2006

59

Management of a neglected anterior dislocation of the elbow associated with a malunited shear fracture of the olecranon in a child in Malawi: The treatment of a deformity by correction at the site of the deformity

Alistair Tindall, Richard N. Brueton

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 105 KB

english, 2005

60

A Novel GPR56 Mutation Causes Bilateral Frontoparietal Polymicrogyria

Rong Luo, Hye Min Yang, Zhaohui Jin, Dicky J.J. Halley, Bernard S. Chang, Lesley MacPherson, Louise Brueton, Xianhua Piao

Journal:

Pediatric Neurology

Année:

2011

Langue:

english

Fichier:

PDF, 672 KB

english, 2011

61

Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease

E. Meyer, M.A. Kurian, N.V. Morgan, A. McNeill, S. Pasha, L. Tee, R. Younis, A. Norman, M.S. van der Knaap, E. Wassmer, R.C. Trembath, L. Brueton, E.R. Maher

Journal:

Molecular Genetics and Metabolism

Année:

2011

Langue:

english

Fichier:

PDF, 755 KB

english, 2011

62

Progressive multilayered banded skin in Winchester syndrome

Rachel U Sidwell, Louise A Brueton, Sophie A Grabczynska, Nick Francis, Robert C.D Staughton

Journal:

Journal of the American Academy of Dermatology

Année:

2004

Langue:

english

Fichier:

PDF, 256 KB

english, 2004

63

Higher specialist training in paediatrics

Journal:

Current Paediatrics

Année:

2001

Langue:

english

Fichier:

PDF, 129 KB

english, 2001

64

Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome

Frances R. Goodman, Chiara Bacchelli, Angela F. Brady, Louise A. Brueton, Jean-Pierre Fryns, Douglas P. Mortlock, Jeffrey W. Innis, Lewis B. Holmes, Alan E. Donnenfeld, Murray Feingold, Frits A. Beeme

Journal:

The American Journal of Human Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 312 KB

english, 2000

65

Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome

Neil V. Morgan, Louise A. Brueton, Phillip Cox, Marie T. Greally, John Tolmie, Shanaz Pasha, Irene A. Aligianis, Hans van Bokhoven, Tamas Marton, Lihadh Al-Gazali, Jenny E.V. Morton, Christine Oley, C

Journal:

The American Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 401 KB

english, 2006

66

Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen

A. Vincent, C. Newland, D. Beeson, S. Riemersma, J. Newsom-Davis, L. Brueton, S.M. Huson

Journal:

Année:

1995

Langue:

english

Fichier:

PDF, 296 KB

english, 1995

67

Polydipsia in infant with oesophagitis

M. Eltumi, D.M. Mathieson, M.J. Brueton, I.Z. Kovar

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 173 KB

english, 1996

68

Homozygous nonsense mutation in the insulin receptor gene in infant with leprechaunism

A. Krook, S. O'Rahilly, L. Brueton

Journal:

Année:

1993

Langue:

english

Fichier:

PDF, 325 KB

english, 1993

69

Fetal acetylcholine receptor function reduced by serum from asymptomatic mother with history of fetal arthrogryposis

Angela Vincent, Sietske Riemersma, John Newson-Davis, Louise Brueton

Journal:

Journal of Neuroimmunology

Année:

1994

Langue:

english

Fichier:

PDF, 156 KB

english, 1994

70

Hypoplastic thumb in Gorlin's syndrome

A. Kansal, L. Brueton, A. Lahiri, R. Lester

Journal:

Journal of Plastic, Reconstructive & Aesthetic Surgery

Année:

2007

Langue:

english

Fichier:

PDF, 151 KB

english, 2007

71

Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia

I. Quack, B. Vonderstrass, M. Stock, AS Aylsworth, A. Becker, L. Brueton, PJ Lee, F. Majewski, JB Mulliken, M. Suri, M. Zenker, S. Mundlos, F. Otto

Journal:

The American Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 355 KB

english, 1999

72

Dysmorphology at a distance: results of a web-based diagnostic service

Douzgou, S, Clayton-Smith, J, Gardner, S, Day, R, Griffiths, P, Strong, K, Amiel, J, Baraitser, M, Brueton, L, Brunner, H, Chrzanowska, K, Dallapiccola, B, del Campo Casanelles, M, Devriendt, K, Donna

Journal:

European Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 298 KB

english, 2014

73

Axenfeld-Rieger syndrome: Further clinical and array delineation of four unrelated patients with a 4q25 microdeletion

Titheradge, Hannah, Togneri, Fiona, McMullan, Dominic, Brueton, Louise, Lim, Derek, Williams, Denise

Journal:

American Journal of Medical Genetics Part A

Année:

2014

Langue:

english

Fichier:

PDF, 197 KB

english, 2014

74

UNSUSPECTED GIARDIASIS

Joss, Vanda, Brueton, MartinJ.

Journal:

Année:

1981

Langue:

english

Fichier:

PDF, 139 KB

english, 1981

75

OPHTHALMIA IN THE METROPOLITAN PAUPER SCHOOLS.

Sullivan, P.B., Brueton, M.J.

Journal:

Année:

1875

Langue:

english

Fichier:

PDF, 374 KB

english, 1875

76

MANCHESTER.

Evans, N., Brueton, M.J., Turner, P.J., Mcneish, A.S.

Journal:

Année:

1894

Langue:

english

Fichier:

PDF, 426 KB

english, 1894

77

BACTERIAL CULTURE OF JEJUNAL MUCOSA IN CHILDHOOD CŒLIAC DISEASE

Evans, N., Brueton, M.J., Turner, P.J., Mcneish, A.S.

Journal:

Année:

1975

Langue:

english

Fichier:

PDF, 322 KB

english, 1975

78

HYPERPHENYLALANAEMIA IN PARENTERALLY FED NEWBORN INFANTS

Mitton, S.G., Burston, D., Brueton, M.J.

Journal:

Année:

1988

Langue:

english

Fichier:

PDF, 310 KB

english, 1988

79

Genetic counselling for cystic fibrosis based upon mutation/haplotype analysis

Watson, Eila, Williamson, Bob, Brueton, Louise, Winter, Robin

Journal:

Année:

1990

Langue:

english

Fichier:

PDF, 348 KB

english, 1990

80

DOES CHLOROQUINE CAUSE HYPOGLYCAEMIA IN THE ABSENCE OF CLINICAL MALARIA?

Ogbuokiri, J.E., Brueton, M.J., Greenwood, B.M., White, N.J., Miller, K.D., Marsh, K., Berry, C.D., Turner, R.C., Williamson, D.H., Brown, J.

Journal:

Année:

1987

Langue:

english

Fichier:

PDF, 322 KB

english, 1987

81

Epidermal growth factor in necrotising enteritis

Sullivan, PeterB., Brueton, MartinJ., Tabara, ZeidB., Goodlad, RobertA., Lee, ChungY., Wright, NicholasA.

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 310 KB

english, 1991

82

Forty-eight glomus tumours of the hand

Gandon, F., Legaillard, Ph., Brueton, R., Le Viet, D., Foucher, G.

Journal:

Annales de Chirurgie de la Main et du Membre Supérieur

Année:

1992

Langue:

english

Fichier:

PDF, 1.79 MB

english, 1992

83

Fetal acetylcholine receptor function reduced by serum from asymptomatic mother with history of fetal arthrogryposis

Vincent, Angela, Riemersma, Sietske, Hawke, Simon, Newsom-Davis, John, Brueton, Louise

Journal:

Neuromuscular Disorders

Année:

1994

Langue:

english

Fichier:

PDF, 58 KB

english, 1994

84

A Malawian child meets an English surgeon

Richard Brueton

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 314 KB

english, 2010

85

Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?

Brueton, L A, Dillon, M J, Winter, R M

Journal:

Journal of Medical Genetics

Année:

1990

Langue:

english

Fichier:

PDF, 946 KB

english, 1990

86

A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype

Zweier, C., Kraus, C., Brueton, L., Cole, T., Degenhardt, F., Engels, H., Gillessen-Kaesbach, G., Graul-Neumann, L., Horn, D., Hoyer, J., Just, W., Rauch, A., Reis, A., Wollnik, B., Zeschnigk, M., Lud

Journal:

Journal of Medical Genetics

Année:

2013

Langue:

english

Fichier:

PDF, 1.33 MB

english, 2013

87

Mutations in GRIP1 cause Fraser syndrome

Vogel, M. J., van Zon, P., Brueton, L., Gijzen, M., van Tuil, M. C., Cox, P., Schanze, D., Kariminejad, A., Ghaderi-Sohi, S., Blair, E., Zenker, M., Scambler, P. J., Ploos van Amstel, H. K., van Haels

Journal:

Journal of Medical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 452 KB

english, 2012

88

Measuring the impact of methodological research at the medical research council clinical trials unit hub for trials methodology research

Valerie Brueton,Claire Vale,Rachel Jinks,Babak Oskooei,Jayne Tierney

Journal:

Année:

2013

Langue:

english

Fichier:

PDF, 121 KB

english, 2013

89

THE SYNTHESIS OF 3-O-[(BENZYLTHIO)CARBONYL]-β-D-GLUCOPYRANOSE AND METHYL 2,4,6-TRI-O-BENZOYL-α AND β-D-GLUCOPYRANOSIDES

Wlllard, J. J., Brimacombe, J. S., Brueton, R. P.

Journal:

Canadian Journal of Chemistry

Année:

1964

Langue:

english

Fichier:

PDF, 385 KB

english, 1964

90

Bristol and Bath Regional Planning Scheme

L., W. S., Abercrombie, Patrick, Brueton, Bertrand F.

Journal:

The Geographical Journal

Année:

1931

Langue:

english

Fichier:

PDF, 330 KB

english, 1931

91

Guidelines for the diagnosis and management of cow's milk protein allergy in infants

Vandenplas, Y., Brueton, M., Dupont, C., Hill, D., Isolauri, E., Koletzko, S., Oranje, A. P, Staiano, A.

Journal:

Archives of Disease in Childhood

Année:

2007

Langue:

english

Fichier:

PDF, 592 KB

english, 2007

92

Hepatic dysfunction in association with pancreatic insufficiency and cyclical neutropenia. Shwachman-Diamond syndrome.

Brueton, M J, Mavromichalis, J, Goodchild, M C, Anderson, C M

Journal:

Archives of Disease in Childhood

Année:

1977

Langue:

english

Fichier:

PDF, 654 KB

english, 1977

93

Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features.

Brueton, L A, Barber, J C, Huson, S M, Winter, R M

Journal:

Journal of Medical Genetics

Année:

1989

Langue:

english

Fichier:

PDF, 354 KB

english, 1989

94

Energy and nutrient intakes in cystic fibrosis.

Buchdahl, R M, Fulleylove, C, Marchant, J L, Warner, J O, Brueton, M J

Journal:

Archives of Disease in Childhood

Année:

1989

Langue:

english

Fichier:

PDF, 822 KB

english, 1989

95

The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.

Brueton, L A, van Herwerden, L, Chotai, K A, Winter, R M

Journal:

Journal of Medical Genetics

Année:

1992

Langue:

english

Fichier:

PDF, 745 KB

english, 1992

96

Should mothers with cystic fibrosis breast feed?

Stead, R J, Brueton, M J, Hodson, M E, Batten, J C

Journal:

Archives of Disease in Childhood

Année:

1987

Langue:

english

Fichier:

PDF, 141 KB

english, 1987

97

CHRNG genotype-phenotype correlations in the multiple pterygium syndromes

Vogt, J., Morgan, N. V., Rehal, P., Faivre, L., Brueton, L. A., Becker, K., Fryns, J.-P., Holder, S., Islam, L., Kivuva, E., Lynch, S. A., Touraine, R., Wilson, L. C., MacDonald, F., Maher, E. R.

Journal:

Journal of Medical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 324 KB

english, 2012

98

Allergic bronchopulmonary aspergillosis complicating cystic fibrosis in childhood.

Brueton, M J, Ormerod, L P, Shah, K J, Anderson, C M

Journal:

Archives of Disease in Childhood

Année:

1980

Langue:

english

Fichier:

PDF, 1.99 MB

english, 1980

99

Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

Brueton, L A, Huson, S M, Farren, B, Winter, R M

Journal:

Journal of Medical Genetics

Année:

1990

Langue:

english

Fichier:

PDF, 1.80 MB

english, 1990

100

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Brueton, L A, Chotai, K A, van Herwerden, L, Schinzel, A, Winter, R M

Journal:

Journal of Medical Genetics

Année:

1992

Langue:

english

Fichier:

PDF, 446 KB

english, 1992