المؤلفون: Khan, Faisel, Little, Julian, Aleotti, Valentina, Mossey, Peter, Steegers-Theunissen, Régine P. M., Autelitano, Luca, Meazzini, Maria Costanza, Ravaei, Amin, Rubini, Michele

المصدر: Khan , F , Little , J , Aleotti , V , Mossey , P , Steegers-Theunissen , R P M , Autelitano , L , Meazzini , M C , Ravaei , A & Rubini , M 2019 , ' LINE-1 methylation in cleft lip tissues : influence of infant MTHFR c.677C >T genotype ' , Oral Diseases , vol. 25 , no. 6 , pp. 1668-1671 . https://doi.org/10.1111/odi.13136Test

مصطلحات موضوعية: DNA methylation, LINE-1, MTHFR c.677C>T, non-syndromic cleft lip with or without cleft palate, Humans, Genotype, Infant, Case-Control Studies, Polymorphism, Genetic, Methylenetetrahydrofolate Reductase (NADPH2)/genetics, Cleft Lip/genetics, Single Nucleotide, Cleft Palate/genetics, MTHFR c.677C > T, /dk/atira/pure/subjectarea/asjc/3500/3500, name=General Dentistry, /dk/atira/pure/subjectarea/asjc/2700/2733, name=Otorhinolaryngology

وصف الملف: application/pdf

العلاقة: https://discovery.dundee.ac.uk/en/publications/75c09fce-7a41-42c3-a1c0-9930594e29c6Test

الإتاحة: https://doi.org/10.1111/odi.13136Test
https://discovery.dundee.ac.uk/en/publications/75c09fce-7a41-42c3-a1c0-9930594e29c6Test
https://discovery.dundee.ac.uk/ws/files/34825983/Khan_et_al_2019_Oral_Diseases.pdfTest
http://www.scopus.com/inward/record.url?scp=85067847942&partnerID=8YFLogxKTest

المؤلفون: Jafar Sabbagh, Heba, Innes, Nicola, Edris Ahmed, Sherif, Butali, Azeez, Abdulbaset Alnamnakani, Eman, Rabah, Sari, Hamdan, Mustafa A., Alhamlan, Nasir, Abdulhameed, Fatma D., Hassan, Mona Hassan Ahmed, Bassam Al Mahdi, Hadiah, Alamoudi, Najlaa M., Alaki, Sumer M., Mossey, Peter

المصدر: Jafar Sabbagh , H , Innes , N , Edris Ahmed , S , Butali , A , Abdulbaset Alnamnakani , E , Rabah , S , Hamdan , M A , Alhamlan , N , Abdulhameed , F D , Hassan , M H A , Bassam Al Mahdi , H , Alamoudi , N M , Alaki , S M & Mossey , P 2019 , ' Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Non-Syndromic Orofacial Cleft in Saudi Arabian Patients ' , Genetic Testing and Molecular Biomarkers , vol. 23 , no. ....

مصطلحات موضوعية: cleft lip, cleft palate, consanguinity, etiology, VAX1, Genetic Testing, Humans, Genetic Predisposition to Disease/genetics, Infant, Male, Case-Control Studies, Saudi Arabia, Polymorphism, Single Nucleotide/genetics, Adult, Female, Cleft Palate/genetics, Newborn, Genome-Wide Association Study, Genotype, Transcription Factors/genetics, Genetic Heterogeneity, Phenotype, Alleles, Homeodomain Proteins/genetics, Family, Cleft Lip/genetics, Brain/abnormalities, /dk/atira/pure/subjectarea/asjc/2700/2716, name=Genetics(clinical)

وصف الملف: application/pdf

العلاقة: https://discovery.dundee.ac.uk/en/publications/22429bcd-e4c2-40c7-accc-2d87e0e1cec9Test

الإتاحة: https://doi.org/10.1089/gtmb.2018.0207Test
https://discovery.dundee.ac.uk/en/publications/22429bcd-e4c2-40c7-accc-2d87e0e1cec9Test
https://discovery.dundee.ac.uk/ws/files/29130559/Sabbagh_et_al._2c_2018_VAX1.pdfTest
http://www.scopus.com/inward/record.url?scp=85059915202&partnerID=8YFLogxKTest

المؤلفون: Khan, Mohammad Faisal Jamal, Little, Julian, Mossey, Peter, Steegers-Theunissen, Regine P. M., Bonsi, Martina, Andreasi, Rita Bassi, Rubini, Michele

المصدر: Khan , M F J , Little , J , Mossey , P , Steegers-Theunissen , R P M , Bonsi , M , Andreasi , R B & Rubini , M 2018 , ' Association between a common missense variant in LOXL3 gene and the risk of non-syndromic cleft palate ' , Congenital Anomalies , vol. 58 , no. 4 , pp. 136-140 . https://doi.org/10.1111/cga.12288Test

مصطلحات موضوعية: cleft palate, lysyl oxidase like 3, missense variant, non-syndromic, Genetic Predisposition to Disease, Amino Acid Oxidoreductases/genetics, Humans, Genotype, Male, Mutation, Missense, Case-Control Studies, Cleft Lip/epidemiology, Cleft Palate/epidemiology, Europe/epidemiology, Female, Polymorphism, Single Nucleotide, Infant, Newborn, /dk/atira/pure/subjectarea/asjc/2700/2700, name=General Medicine

وصف الملف: application/pdf

العلاقة: https://discovery.dundee.ac.uk/en/publications/26933f5d-a770-4fd9-9368-5cffab7f6d61Test

الإتاحة: https://doi.org/10.1111/cga.12288Test
https://discovery.dundee.ac.uk/en/publications/26933f5d-a770-4fd9-9368-5cffab7f6d61Test
https://discovery.dundee.ac.uk/ws/files/27237957/Revised_Manuscript_ID_CGA_12_2017_125.R1.pdfTest