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1
Gardner and Sutherland's chromosome abnormalities and genetic counseling
Gardner and Sutherland's chromosome abnormalities and genetic counseling
Material Type:
Livro 		Adicionar ao Meu Espaço

Gardner and Sutherland's chromosome abnormalities and genetic counseling

R. J. McKinlay Gardner David J Amor

New York Oxford University Press 2018

Localização: IB - Instituto de Biociências    (QH431 G228g 5.ed. )(Acessar)

2
Chromosome abnormalities and genetic counseling
Chromosome abnormalities and genetic counseling
Material Type:
Livro 		Adicionar ao Meu Espaço

Chromosome abnormalities and genetic counseling

R. J. M. Gardner Grant R Sutherland

New York Oxford University Press 1996

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (575:61 G228c 27492 )(Acessar)

3
Chromosome abnormalities and genetic counseling
Chromosome abnormalities and genetic counseling
Material Type:
Livro 		Adicionar ao Meu Espaço

Chromosome abnormalities and genetic counseling

R. J. M. Gardner Grant R Sutherland

New York Oxford University Press 2004

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (575:61 G228c3 )(Acessar)

4
Chromosome abnormalities and genetic counseling
Chromosome abnormalities and genetic counseling
Material Type:
Livro 		Adicionar ao Meu Espaço

Chromosome abnormalities and genetic counseling

R. J. M Gardner Grant R Sutherland; Lisa G Shaffer

Oxford Oxford University Press New York c2012

Item não circula. Consulte sua biblioteca.(Acessar)

5
A Handbook of neuropsychological assessment
A Handbook of neuropsychological assessment
Material Type:
Livro 		Adicionar ao Meu Espaço

A Handbook of neuropsychological assessment

John R Crawford 1957-; Denis M Parker; William W McKinlay

Hove, UK ; Hillsdale, USA L. Erlbaum Associates c1992

Localização: ICB - Inst. Ciências Biomédicas    (WL102 H236 1992 ex.1 )(Acessar)

6
Exposure to static and low frequency electromagnetic fields, biological effects and health consequences (0-100 kHz) review of the scientific evidence on dosimetry, biological effects, epidemiological observations, and health consequences concerning exposure to static and low frequency electromagnetic fields (0-100 kHz)
Exposure to static and low frequency electromagnetic fields, biological effects and health consequences (0-100 kHz) review of the scientific evidence on dosimetry, biological effects, epidemiological observations, and health consequences concerning exposure to static and low frequency electromagnetic fields (0-100 kHz)
Material Type:
Livro 		Adicionar ao Meu Espaço

Exposure to static and low frequency electromagnetic fields, biological effects and health consequences (0-100 kHz) review of the scientific evidence on dosimetry, biological effects, epidemiological observations, and health consequences concerning exposure to static and low frequency electromagnetic fields (0-100 kHz)

Rüdiger Matthes; Alastair F McKinlay; Jürgen H Bernhardt; Paolo Vecchia; Bernard Veyret

Oberschleißheim International Comission on Non-Ionizing Radiation Protection 2003

Localização: FSP - Faculdade de Saúde Pública    (363.7 37 )(Acessar)

7
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

Nguyen, Ngoc Minh Phuong ; Khawajkie, Yassemine ; Mechtouf, Nawel ; Rezaei, Maryam ; Breguet, Magali ; Kurvinen, Elvira ; Jagadeesh, Sujatha ; Solmaz, Asli Ece ; Aguinaga, Monica ; Hemida, Reda ; Harma, Mehmet Ibrahim ; Rittore, Cécile ; Rahimi, Kurosh ; Arseneau, Jocelyne ; Hovanes, Karine ; Clisham, Ronald ; Lenzi, Tiffanee ; Scurry, Bonnie ; Addor, Marie-Claude ; Bagga, Rashmi ; Nendaz, Genevieve Girardet ; Finci, Vildana ; Poke, Gemma ; Grimes, Leslie ; Gregersen, Nerine ; York, Kayla ; Bolze, Pierre-Adrien ; Patel, Chirag ; Mozdarani, Hossein ; Puechberty, Jacques ; Scotchie, Jessica ; Fardaei, Majid ; Harma, Muge ; Gardner, R. J. McKinlay ; Sahoo, Trilochan ; Dudding-Byth, Tracy ; Srinivasan, Radhika ; Sauthier, Philippe ; Slim, Rima

Modern pathology, 2018-07, Vol.31 (7), p.1116-1130 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
Material Type:
Artigo 		Adicionar ao Meu Espaço

Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25

Barbier, Mathieu ; Bahlo, Melanie ; Pennisi, Alessandra ; Jacoupy, Maxime ; Tankard, Rick M. ; Ewenczyk, Claire ; Davies, Kayli C. ; Lino‐Coulon, Patricia ; Colace, Claire ; Rafehi, Haloom ; Auger, Nicolas ; Ansell, Brendan R. E. ; Stelt, Ivo ; Howell, Katherine B. ; Coutelier, Marie ; Amor, David J. ; Mundwiller, Emeline ; Guillot‐Noël, Lena ; Storey, Elsdon ; Gardner, R. J. McKinlay ; Wallis, Mathew J. ; Brusco, Alfredo ; Corti, Olga ; Rötig, Agnès ; Leventer, Richard J. ; Brice, Alexis ; Delatycki, Martin B. ; Stevanin, Giovanni ; Lockhart, Paul J. ; Durr, Alexandra

Annals of neurology, 2022-07, Vol.92 (1), p.122-137 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing
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Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing

McGillivray, George ; Rosenfeld, Jill A ; McKinlay Gardner, R. J. ; Gillam, Lynn H.

Prenatal diagnosis, 2012-04, Vol.32 (4), p.389-395 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

Texto completo disponível

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10
TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families
TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families
Material Type:
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TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

Andreucci, Elena ; Aftimos, Salim ; Alcausin, Melanie ; Haan, Eric ; Hunter, Warwick ; Kannu, Peter ; Kerr, Bronwyn ; McGillivray, George ; McKinlay Gardner, R J ; Patricelli, Maria G ; Sillence, David ; Thompson, Elizabeth ; Zacharin, Margaret ; Zankl, Andreas ; Lamandé, Shireen R ; Savarirayan, Ravi

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.37-37 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

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Deste Autor:

  1. Gardner, R
  2. Sutherland, G
  3. Vecchia, P
  4. Matthes, R
  5. Parker, D

Neste Assunto:

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

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

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