Linkage study of best’s vitelliform macular dystrophy (VMD2) in a large north american family

Human Heredity

Volumn 46, Issue 4, 1996, Pages 211-220

  Hou, Yu Chih ^a   Richards, Julia E ^a,b   Bingham, Eve L ^a   Pawar, Hemant ^a   Scott, Kathy ^a   Segal, Meridee ^a   Lunetta, Kathryn L ^c   Boehnke, Michael ^c   Sieving, Paul A ^a  

^a VA Ann Arbor Healthsystem   (United States)

^b OptumInsight (Formerly Ingenix i3 Drug Safety)   (United States)

^c UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Eye disease; Genetic linkage; Human chromosome 11; Macular degeneration

Indexed keywords

ARTICLE; CLINICAL ARTICLE; FEMALE; GENE; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC MARKER; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MALE; NORTH AMERICA; RETINA MACULA VITELLIFORM DEGENERATION;

ADULT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; DNA MUTATIONAL ANALYSIS; ELECTROOCULOGRAPHY; EYE PROTEINS; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GENOTYPE; HUMANS; LINKAGE (GENETICS); MACULAR DEGENERATION; MALE; MEMBRANE PROTEINS; MIDDLE AGED; NORTH AMERICA; PEDIGREE; VISUAL ACUITY;

EID: 0029948714     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000154356     Document Type: Article

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