Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes - Kamnasaran, Deepak; Chen, Chih-Ping; Devriendt, Koenraad; Mehta, Lakshmi; Cox, Diane W. (Genomics (San Diego, Calif.), 2005)
Keywords: Animals; Base Sequence; Biological and medical sciences; Blotting, Northern; Brain; Brain - metabolism; Carrier Proteins - genetics; Chromosome Deletion; Chromosome Walking; Chromosomes, Human, Pair 14 - genetics; Computational Biology; Contig Mapping; Craniofacial; Disease genes; DNA Primers; DNA, Complementary - genetics; Fetus - metabolism; Fundamental and applied biological sciences. Psychology; Gene Expression; Genes. Genome; Genetics of eukaryotes. Biological and molecular evolution; Holoprosencephaly - genetics; Humans; In Situ Hybridization; Malformations of the nervous system; Medical sciences; Mice; Mice, Inbred C57BL; Midline defect; Molecular and cellular biology; Molecular genetics; Molecular Sequence Data; Neurology; Nucleic Acid Amplification Techniques; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Sorting Nexins; Vesicular Transport Proteins; Brain; Midline defect; Craniofacial; Disease genes; Human; Arhinencephaly; Nervous system diseases; Genomics; Chromosome; Congenital disease; Cerebral disorder; Characterization; Malformation; Central nervous system disease; Candidate gene; Locus