about
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from ScandinaviaMedical sequencing of candidate genes for nonsyndromic cleft lip and palateCharacterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateA novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansMutations in IRF6 cause Van der Woude and popliteal pterygium syndromesCandidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for cleftsPrevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeA genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateImpaired FGF signaling contributes to cleft lip and palateInterferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palateGenetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications.Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate'Information is information': a public perspective on incidental findings in clinical and research genome-based testingResearcher and institutional review board chair perspectives on incidental findings in genomic research.Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia.Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.Informed consent and genomic incidental findings: IRB chair perspectives.A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairsMutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice.Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsIntegrating genomics into undergraduate nursing education.A practical first step to integrating genetics into the curriculum.Five-Year Bibliometric Review of Genomic Nursing Science Research.Educating future nursing scientists: Recommendations for integrating omics content in PhD programs.Evaluation of the Perception of Risk Factors for Type 2 Diabetes Instrument in an At-Risk, Nondiabetic Population.Women's knowledge and use of prenatal screening tests.The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations.The importance of patient engagement.Maternal vitamin B-6 and folate status and risk of oral cleft birth defects in the Philippines.Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families.Filipino explanatory models of cleft lip with or without cleft palate.The International Society of Nurses in Genetics (ISONG) 2015 World Congress: Epigenetics Across the Life Span.PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.Integrating genetics and genomics into nursing curricula: you can do it too!
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P50
description
hulumtuese
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researcher
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հետազոտող
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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Sandra Daack-Hirsch
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P106
P1153
6603278936
P21
P31
P496
0000-0003-1192-7154