Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5

BMC Genetics

Volumn 5, Issue , 2004, Pages

  Bajaj, Vineeta ^a   Markandaya, Manjunath ^a   Krishna, Lingegowda ^b   Kumar, Arun ^a  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b KEMPEGOWDA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME PROTEIN; COMPLEMENTARY DNA; DNA; MEMBRANE PROTEIN; SLC22A18AS PROTEIN, HUMAN;

ABORTION; ALLELE; ARTICLE; BRAIN; CHROMOSOME 11P; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; EXON; FETUS; FETUS (ANATOMY); FETUS LIVER; FETUS LUNG; GENE EXPRESSION; GENE LOCATION; GENOME IMPRINTING; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; KIDNEY; NUCLEOTIDE SEQUENCE; PLACENTA; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; CHEMISTRY; CHROMOSOME 11; GENE EXPRESSION REGULATION; GENETICS; HETEROZYGOTE; HETEROZYGOTE DETECTION; METABOLISM; METHODOLOGY; POINT MUTATION; SPONTANEOUS ABORTION;

ABORTION, SPONTANEOUS; ALLELES; CHROMOSOMES, HUMAN, PAIR 11; DNA; DNA MUTATIONAL ANALYSIS; FETUS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENOMIC IMPRINTING; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMANS; MEMBRANE PROTEINS; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 25444477817     PISSN: 14712156     EISSN: None     Source Type: Journal    
DOI: 10.1186/1471-2156-5-13     Document Type: Article

References (12)

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