Genomic approaches for studying craniofacial disorders

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 163, Issue 4, 2013, Pages 218-231

  Khandelwal, Kriti D ^a   van Bokhoven, Hans ^a   Roscioli, Tony ^a   Carels, Carine E L ^a   Zhou, Huiqing ^b  

^a Department of Orthodontics and Craniofacial Biology ^*

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

DNA microarrays; Genomics; NGS; Orofacial clefts

Indexed keywords

COMPLEMENTARY DNA; FIBROBLAST GROWTH FACTOR RECEPTOR 2; INTERFERON REGULATORY FACTOR 6; MICRORNA; NECTIN 1; NUCLEOTIDE; TRANSCRIPTION FACTOR MSX1; UNTRANSLATED RNA;

ARTICLE; AURICULOCONDYLAR SYNDROME; BARTSOCAS PAPAS SYNDROME; CAVALLAZZI SYNDROME; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; CRANIOFACIAL MALFORMATION; DYSOSTOSIS; EEC SYNDROME; EXOME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE INTERACTION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOMICS; GENOTYPE ENVIRONMENT INTERACTION; HARTSFIELD SYNDROME; HUMAN; INHERITANCE; KABUKI MAKEUP SYNDROME; LINKAGE ANALYSIS; METAPHASE CHROMOSOME; NAGER ACROFACIAL DYSOSTOSIS; NONHUMAN; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; BRAIN; CLEFT LIP; CLEFT PALATE; GENETIC LINKAGE; GENETICS; HIGH THROUGHPUT SEQUENCING; PATHOLOGY;

BRAIN; CLEFT LIP; CLEFT PALATE; CRANIOFACIAL ABNORMALITIES; DNA COPY NUMBER VARIATIONS; EXOME; GENETIC LINKAGE; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS;

EID: 84886245186     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31379     Document Type: Article

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