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1دورية أكاديمية
المؤلفون: Richardson, R, Donnai, D, Meire, F, Dixon, M J
المصدر: Richardson , R , Donnai , D , Meire , F & Dixon , M J 2004 , ' Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly ' , Journal of Medical Genetics , vol. 41 , no. 1 , pp. 60-7 .
مصطلحات موضوعية: Abnormalities, Multiple, Amino Acid Sequence, Animals, Cattle, Connexin 43, Craniofacial Abnormalities, Cricetinae, Embryo, Mammalian, Eye Abnormalities, Fingers, Gene Expression Regulation, Developmental, Humans, Mice, Molecular Sequence Data, Mutation, Missense, Phenotype, Rats, Sequence Alignment, Syndactyly, Syndrome, Tooth Abnormalities
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2دورية أكاديمية
المؤلفون: Narbay, G, Meire, F, Verloes, A, Casteels, Ingele, Devos, Lily
مصطلحات موضوعية: Abnormalities, Multiple, Brain, Child, Preschool, Eye Abnormalities, Face, Humans, Infant, Newborn, Male, Scalp, Syndrome
العلاقة: Bulletin de la Société Belge d'Ophtalmologie vol:261 pages:65-70; https://lirias.kuleuven.be/handle/123456789/531591Test
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3
المؤلفون: Casteels, I., Devos, E., Meire, F., Narbay, G., Alain VERLOES
المصدر: Europe PubMed Central
Scopus-Elsevierمصطلحات موضوعية: Male, Scalp, Child, Preschool, Face, Infant, Newborn, Brain, Humans, Abnormalities, Multiple, Eye Abnormalities, Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::75b28c140db67329cd210dc56e16ed47Test
http://europepmc.org/abstract/med/9009364Test