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1
Haplotypes linked to the X chromosome in paternity investigation in incomplete cases
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Artigo de Congresso
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Haplotypes linked to the X chromosome in paternity investigation in incomplete cases

I. C. D. Alcarás Aguinaldo Luiz Simões; Brazilian-International Congress of Genetics (62. 2016 Caxambu)

Abstracts Caxambu : SBG, 2016

Caxambu SBG 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2875788 Estantes Deslizantes )(Acessar)

2
P82 Estimating the prevalence of Wilson’s disease using routine laboratory and clinical data
Material Type:
Artigo
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P82 Estimating the prevalence of Wilson’s disease using routine laboratory and clinical data

Wijayasiri, Pramudi ; Hayre, J ; Nicholson, Ed S ; Kaye, Philip ; Venkatachalapathy, Suresh V ; Eddowes, Peter J ; Wilkes, Emilie ; Guha, Indra N ; James, Martin ; Ryder, Stephen D ; Aithal, Guru P ; Pearce, Fiona ; Aravinthan, Aloysious D

Gut, 2020-09, Vol.69 (Suppl 1), p.A46-A46 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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3
IDDF2020-ABS-0209 Asian prevalent allele at ABCB5 SNP Rs10254317 associates with hepatocellular carcinoma (HCC) risk and adverse clinical outcomes
Material Type:
Artigo
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IDDF2020-ABS-0209 Asian prevalent allele at ABCB5 SNP Rs10254317 associates with hepatocellular carcinoma (HCC) risk and adverse clinical outcomes

Yeung, Philip Chun ; Chong, Charing Ching-Ning ; Cheung, Tan To ; Chai Ng, Kelvin Kwok ; Lai, Paul Bo San ; Cheung, Siu Tim

Gut, 2020-11, Vol.69 (Suppl 2), p.A26-A26 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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4
GP17 Distribution of non-functional allele of CYP2D6 gene (rs1065852) among buryat adolescents
Material Type:
Artigo
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GP17 Distribution of non-functional allele of CYP2D6 gene (rs1065852) among buryat adolescents

Bairova, Tatyana ; Ievleva, Ksenia ; Bodonova, Lyudmila ; Rychkova, Lyubov

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A36 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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5
OC65 Normative neonatal facial bio-metrics in the united arab emirates for non-invasive early detection of genetic disorder
Material Type:
Artigo
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OC65 Normative neonatal facial bio-metrics in the united arab emirates for non-invasive early detection of genetic disorder

Zaabi, Olfat Al ; Porras, Antonio R ; Khajeh, Safyia Saif Al ; Moghanni, Yamen El ; Salah, Mona ; Ismail, Ahmed Abdelwahab ; Mazar, Asma Abdelrahman Al ; Rahman, Mona Abdul ; Helmi, Rola ; Wahab, Luay A ; Eleimy, Hussein ; Ummerkhan, Anshad ; Linguraru, Marius George

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A27 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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6
P128 A retrospective audit of microarray testing performed in the developmental clinic at a tertiary paediatric centre
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Artigo
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P128 A retrospective audit of microarray testing performed in the developmental clinic at a tertiary paediatric centre

McGrath, Thomas ; Kelly, Stephanie ; Gallagher, Louise ; Curtis, Emma

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A207 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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Deste Autor:

  1. Alcarás, I
  2. Simões, A
  3. Brazilian-International Congress of Genetics

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