Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity

Molecular Vision

Volumn 11, Issue , 2005, Pages 501-508

  Hutcheson, Kelly A ^a   Palaru, Prasuna C ^b   Bernstein, Steven L ^c   Koh, Jamie ^b   Rappaport, Eric F ^b   Leach, Richard A ^d   Young, Terri L ^b  

^a CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

^d Teneo Sciences   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE;

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; AFRICAN AMERICAN; ARTICLE; BASE PAIRING; BIRTH WEIGHT; CAUCASIAN; COHORT ANALYSIS; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DISEASE SEVERITY; ETHNIC DIFFERENCE; EXON; FEMALE; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC VARIABILITY; GESTATIONAL AGE; HETEROZYGOSITY; HUMAN; INFANT; INFANT DISEASE; MAJOR CLINICAL STUDY; MALE; NORRIE DISEASE; PATHOGENESIS; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PRIORITY JOURNAL; RACE DIFFERENCE; RETROLENTAL FIBROPLASIA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; WILD TYPE;

3' UNTRANSLATED REGIONS; 5' UNTRANSLATED REGIONS; ADULT; AFRICAN AMERICANS; CASE-CONTROL STUDIES; COHORT STUDIES; DNA TRANSPOSABLE ELEMENTS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; EYE PROTEINS; FEMALE; GENE DELETION; HETEROZYGOTE; HUMANS; INFANT, NEWBORN; MALE; NERVE TISSUE PROTEINS; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINOPATHY OF PREMATURITY; SEVERITY OF ILLNESS INDEX;

EID: 26244442311     PISSN: 10900535     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (26)

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