TY  - GEN
AU  - Cusano,R
AU  - Gangarossa,S
AU  - Forabosco,P
AU  - Caridi,G
AU  - Ghiggeri,G M
AU  - Russo,G
AU  - Iolascon,A
AU  - Ravazzolo,R
AU  - Seri,M
TI  - Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13
SN  - 1018-4813
PY  - 2000///1207
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 22
KW  - DNA
KW  - Eye Abnormalities
KW  - Family Health
KW  - Female
KW  - Genotype
KW  - Haplotypes
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Italy
KW  - Male
KW  - Microsatellite Repeats
KW  - Middle Aged
KW  - Nephritis
KW  - Pedigree
KW  - Syndrome
KW  - Thrombocytopenia
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/sj.ejhg.5200533
ER  -