Clinical Presentation and Genetic Correlation of Patients with Mutations Affecting the FZD4 Gene

Archives of Ophthalmology

Volumn 127, Issue 12, 2009, Pages 1649-1654

  Drenser, Kimberly A ^a   Dailey, Wendelin ^a   Vinekar, Anand ^b   Dalal, Kunal ^a   Capone Jr , Antonio ^a   Trese, Michael T ^a  

^a WILLIAM BEAUMONT HOSPITAL   (United States)

^b POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

FRIZZLED 4 RECEPTOR; FRIZZLED PROTEIN; GENOMIC DNA; UNCLASSIFIED DRUG; FZD4 PROTEIN, HUMAN; G PROTEIN COUPLED RECEPTOR; PRIMER DNA;

ARTICLE; AUTOSOMAL DOMINANT FAMILIAL EXUDATIVE VITREORETINOPATHY; AUTOSOMAL DOMINANT INHERITANCE; CHILDHOOD DISEASE; CHROMOSOME; DNA ISOLATION; FAMILY HISTORY; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CORRELATION; HETEROZYGOTE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEWBORN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETROLENTAL FIBROPLASIA; SCREENING; VITREORETINOPATHY; CHEMISTRY; CHILD; DNA SEQUENCE; EXUDATE; GENETICS; GESTATIONAL AGE; MUTATION; NUCLEOTIDE SEQUENCE;

CHILD; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; EXUDATES AND TRANSUDATES; FRIZZLED RECEPTORS; GESTATIONAL AGE; HUMANS; INFANT; INFANT, NEWBORN; MUTATION; RECEPTORS, G-PROTEIN-COUPLED; RETINOPATHY OF PREMATURITY; SEQUENCE ANALYSIS, DNA; VITREORETINOPATHY, PROLIFERATIVE;

EID: 73349143337     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2009.322     Document Type: Article

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