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Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation
Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation
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Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation

Porntaveetus, T ; Osathanon, T ; Nowwarote, N ; Pavasant, P ; Srichomthong, C ; Suphapeetiporn, K ; Shotelersuk, V

Oral diseases, 2018-05, Vol.24 (4), p.619-627 [Periódico revisado por pares]

Denmark: Wiley Subscription Services, Inc

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12
A mutation of the p63 gene in non-syndromic cleft lip
A mutation of the p63 gene in non-syndromic cleft lip
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A mutation of the p63 gene in non-syndromic cleft lip

Leoyklang, P ; Siriwan, P ; Shotelersuk, V

Journal of medical genetics, 2006-06, Vol.43 (6), p.e28-e28 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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13
Three novel mutations in the PORCN gene underlying focal dermal hypoplasia
Three novel mutations in the PORCN gene underlying focal dermal hypoplasia
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Three novel mutations in the PORCN gene underlying focal dermal hypoplasia

Leoyklang, P ; Suphapeetiporn, K ; Wananukul, S ; Shotelersuk, V

Clinical genetics, 2008-04, Vol.73 (4), p.373-379 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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14
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population
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TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population

Suphapeetiporn, K ; Tongkobpetch, S ; Siriwan, P ; Shotelersuk, V

Clinical genetics, 2007-11, Vol.72 (5), p.478-483 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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15
Significant association between IRF6 820G→A and non-syndromic cleft lip with or without cleft palate in the Thai population
Significant association between IRF6 820G→A and non-syndromic cleft lip with or without cleft palate in the Thai population
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Significant association between IRF6 820G→A and non-syndromic cleft lip with or without cleft palate in the Thai population

Srichomthong, C ; Siriwan, P ; Shotelersuk, V

Journal of medical genetics, 2005-07, Vol.42 (7), p.e46-e46 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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16
SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome
SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome
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SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome

Suphapeetiporn, K ; Srichomthong, C ; Shotelersuk, V

Clinical genetics, 2011-04, Vol.79 (4), p.391-393 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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17
Novel mutations in the FUCA1 gene that cause fucosidosis
Novel mutations in the FUCA1 gene that cause fucosidosis
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Novel mutations in the FUCA1 gene that cause fucosidosis

Panmontha, W ; Amarinthnukrowh, P ; Damrongphol, P ; Desudchit, T ; Suphapeetiporn, K ; Shotelersuk, V

Genetics and molecular research, 2016-09, Vol.15 (3) [Periódico revisado por pares]

Brazil

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18
Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous Mutation
Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous Mutation
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Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous Mutation

Phowthongkum, P. ; Ittiwut, C. ; Shotelersuk, V.

JIMD Reports, Volume 41, 2018-01, Vol.41, p.11-16 [Periódico revisado por pares]

Berlin, Heidelberg: Springer Berlin Heidelberg

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19
Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
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Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip

Shotelersuk, V ; Ittiwut, C ; Siriwan, P ; Angspatt, A

Journal of medical genetics, 2003-05, Vol.40 (5), p.e64-64 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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20
Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondyloepiphyseal dysplasia congenita
Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondyloepiphyseal dysplasia congenita
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Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondyloepiphyseal dysplasia congenita

Sangsin, A ; Srichomthong, C ; Pongpanich, M ; Suphapeetiporn, K ; Shotelersuk, V

Genetics and molecular research, 2016-01, Vol.15 (1) [Periódico revisado por pares]

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Deste Autor:

  1. Patil, S
  2. Paththinige, C
  3. Shotelersuk, V
  4. Muenke, M
  5. Moresco, A

Neste Assunto:

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

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

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