Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation - Osoegawa, K; Vessere, G M; Utami, K H; Mansilla, M A; Johnson, M K; Riley, B M; L’Heureux, J; Pfundt, R; Staaf, J; van der Vliet, W A; Lidral, A C; Schoenmakers, E F P M; et al. (Journal of medical genetics, 2008)
Keywords: Artificial chromosomes; Base Sequence; Basic Medicine; Biological and medical sciences; Child; Chromosome Deletion; Chromosome Mapping; Chromosomes, Artificial, Bacterial - genetics; Chromosomes, Human, Pair 10 - genetics; Chromosomes, Human, Pair 22 - genetics; Chromosomes, Human, Pair 6 - genetics; Cleft Lip - genetics; Cleft Palate - genetics; Cloning; Deoxyribonucleic acid; DNA; DNA - genetics; Facial bones, jaws, teeth, parodontium: diseases, semeiology; Families & family life; Female; Fundamental and applied biological sciences. Psychology; Gene Dosage; Gene loci; General aspects. Genetic counseling; Genetic testing; Genetic Variation; Genetics of eukaryotes. Biological and molecular evolution; Genomes; Humans; Intellectual disabilities; Male; Medical and Health Sciences; Medical Genetics; Medical Genetics and Genomics (including Gene Therapy); Medical sciences; Medicin och hälsovetenskap; Medicinsk genetik; Medicinsk genetik och genomik (Här ingår: Genterapi); Medicinska och farmaceutiska grundvetenskaper; Molecular and cellular biology; Mutation; Non tumoral diseases; Nucleic Acid Hybridization; Otorhinolaryngology. Stomatology; Phenotype; Studies; Syndrome; Iowa; Philippines; Human; Cleft palate; Cleft lip; Stomatology; Pathogenesis; Genomics; Congenital cleft; Identification; Congenital disease; Genetic determinism; Association; Malformation; Genetics; Oral cavity disease; Comparative study