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Refinado por: assunto: Mutation remover
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1
Mutation as cellular process a Ciba Foundation symposium
Mutation as cellular process a Ciba Foundation symposium
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Mutation as cellular process a Ciba Foundation symposium

Symposium on Mutation as Cellular Process (1969 London, England) G. E. W Wolstenholme (Gordon Ethelbert Ward); Maeve O'Connor; Ciba Foundation

London Churchill 1969

Localização: CQ - Conjunto das Químicas    (575.292 W867m ) e outros locais(Acessar)

2
Molecular and environmental aspects of mutagenesis
Molecular and environmental aspects of mutagenesis
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Molecular and environmental aspects of mutagenesis

Rochester International Conference on Environmental Toxicity (6th 1973) Louise Prakash; University of Rochester Dept. of Radiation Biology and Biophysics

Springfield, Ill. Thomas 1974

Localização: ESALQ - Biblioteca Central    (591.1592 M718 27262 )(Acessar)

3
Chemical mutagenesis in mammals and man
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Chemical mutagenesis in mammals and man

Friedrich Vogel 1925-; G Röhrborn; Gesellschaft für Anthropologie und Humangenetik

Berlin New York Springer-Verlag 1970

Localização: CENA - Cent. En. Nuclear na Agricultura    (575.24 V878c 2630 ) e outros locais(Acessar)

4
Genetic damage in man caused by environmental agents
Genetic damage in man caused by environmental agents
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Genetic damage in man caused by environmental agents

Kåre Berg; Norske videnskaps-akademi i Oslo

New York Academic Press 1979

Localização: FSP - Faculdade de Saúde Pública    (573.222 1 )(Acessar)

5
Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect
Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect
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Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect

Qiao, F. ; Wang, Y. ; Zhang, C. ; Zhou, R. ; Wu, Y. ; Wang, C. ; Meng, L. ; Mao, P. ; Cheng, Q. ; Luo, C. ; Hu, P. ; Xu, Z.

Ultrasound in obstetrics & gynecology, 2021-09, Vol.58 (3), p.377-387 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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6
Use of human lymphocyte G0 PCCs to detect intra- and inter-chromosomal aberrations for early radiation biodosimetry and retrospective assessment of radiation-induced effects
Use of human lymphocyte G0 PCCs to detect intra- and inter-chromosomal aberrations for early radiation biodosimetry and retrospective assessment of radiation-induced effects
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Use of human lymphocyte G0 PCCs to detect intra- and inter-chromosomal aberrations for early radiation biodosimetry and retrospective assessment of radiation-induced effects

Ryan, Terri L ; Pantelias, Antonio G ; Terzoudi, Georgia I ; Pantelias, Gabriel E ; Balajee, Adayabalam S Amendola, Roberto

PloS one, 2019-05, Vol.14 (5), p.e0216081 [Periódico revisado por pares]

United States: Public Library of Science

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7
Genotoxic effects of lead: An updated review
Genotoxic effects of lead: An updated review
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Genotoxic effects of lead: An updated review

García-Lestón, Julia ; Méndez, Josefina ; Pásaro, Eduardo ; Laffon, Blanca

Environment international, 2010-08, Vol.36 (6), p.623-636 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2
Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2
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Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2

Gonzalez, Michael ; McLaughlin, Heather ; Houlden, Henry ; Guo, Min ; Yo-Tsen, Liu ; Hadjivassilious, Marios ; Speziani, Fiorella ; Yang, Xiang-Lei ; Antonellis, Anthony ; Reilly, Mary M ; Züchner, Stephan

Journal of neurology, neurosurgery and psychiatry, 2013-11, Vol.84 (11), p.1247-1249 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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9
Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma
Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma
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Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma

Frias, Sara ; Van Hummelen, Paul ; Meistrich, Marvin L ; Wyrobek, Andrew J Drevet, Joël R

PloS one, 2020-12, Vol.15 (12), p.e0242218 [Periódico revisado por pares]

United States: Public Library of Science

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10
AOP report: Development of an adverse outcome pathway for oxidative DNA damage leading to mutations and chromosomal aberrations
AOP report: Development of an adverse outcome pathway for oxidative DNA damage leading to mutations and chromosomal aberrations
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AOP report: Development of an adverse outcome pathway for oxidative DNA damage leading to mutations and chromosomal aberrations

Cho, Eunnara ; Allemang, Ashley ; Audebert, Marc ; Chauhan, Vinita ; Dertinger, Stephen ; Hendriks, Giel ; Luijten, Mirjam ; Marchetti, Francesco ; Minocherhomji, Sheroy ; Pfuhler, Stefan ; Roberts, Daniel J. ; Trenz, Kristina ; Yauk, Carole L.

Environmental and molecular mutagenesis, 2022-03, Vol.63 (3), p.118-134 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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