A recombination outside the BB deletion refines the location of the X- linked retinitis pigmentosa locus RP3

American Journal of Human Genetics

Volumn 59, Issue 1, 1996, Pages 152-158

  Fujita, R ^a   Bingham, E ^a   Forsythe, P ^a   McHenry, C ^a   Aita, V ^a   Navia, B A ^a   Dry, K ^a   Segal, M ^a   Devoto, M ^a   Bruns, G ^a   Wright, A F ^a   Ott, J ^a   Sieving, P A ^a   Swaroop, A ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CROSSING OVER; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; GENE LOCUS; GENETIC LINKAGE; GENETIC RECOMBINATION; GRANULOMATOSIS; HUMAN; HYPERTRANSLUCENT LUNG; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; X CHROMOSOME LINKED DISORDER;

ADULT; BASE SEQUENCE; CHROMOSOME MAPPING; DNA PRIMERS; ELECTRORETINOGRAPHY; FEMALE; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; PEDIGREE; RECOMBINATION, GENETIC; RETINITIS PIGMENTOSA; SEQUENCE DELETION; X CHROMOSOME;

EID: 0029980134     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)