Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

American Journal of Medical Genetics

Volumn 132 A, Issue 3, 2005, Pages 324-328

  Boonen, S E ^a   Stahl, D ^b   Kreiborg, S ^c   Rosenberg, T ^d   Kalscheuer, V ^e   Larsen, L A ^f   Tommerup, N ^f   Brondum Nielsen K ^a   Tumer Z ^f,g  

^a JOHN F KENNEDY INSTITUTE   (Denmark)

^b Dermatology Clinic   (Denmark)

^c UNIVERSITY OF COPENHAGEN   (Denmark)

^d National Eye Clinic for the Visually Impaired Denmark   (Denmark)

^e MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^f UNIVERSITY OF COPENHAGEN   (Denmark)

^g UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

9q; 9q22; Basal cell nevus syndrome; BCNS; FISH; Gorlin syndrome; Interstitial deletion; PTCH; ROR2

Indexed keywords

ADULT; ANAMNESIS; BACTERIAL ARTIFICIAL CHROMOSOME; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; BRAIN TOMOGRAPHY; CASE REPORT; CHROMOSOME 9Q; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL EXAMINATION; CLINICAL FEATURE; CONFERENCE PAPER; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HEMIZYGOSITY; HUMAN; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE 46,XY; MALE; NUCLEOTIDE SEQUENCE; ODONTOGENIC KERATOCYST; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER;

ADULT; BASAL CELL NEVUS SYNDROME; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE;

EID: 11344275232     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30422     Document Type: Conference Paper

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