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Publication : bmc medical genetics
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Academic Journal

Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report.

  • Authors : Wang X; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.; Tan L

Subjects: Asian People/Asian People/Asian People/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Ichthyosis/Ichthyosis/Ichthyosis/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2018 Jul 18; Vol. 19 (1), pp. 120. Date of Electronic Publication: 2018 Jul 18.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report

Subjects: Adult; Male; 0301 basic medicine

  • Source: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)BMC Medical Genetics

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Academic Journal

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis.

Subjects: Algorithms* ; Genome-Wide Association Study*; Dermatitis, Atopic/Dermatitis, Atopic/Dermatitis, Atopic/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2012 Jan 27; Vol. 13, pp. 8. Date of Electronic Publication: 2012 Jan 27.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis

Subjects: lcsh:Internal medicine; Filaggrin mutations; Traits

  • Source: BMC Medical Genetics, Vol 13, Iss 1, p 8 (2012)BMC Medical GeneticsBMC Med. Genet. 13:8 (2012)

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  • 1-4 ل  4 نتائج ل ""Filaggrin Proteins""