TY  - GEN
AU  - Brøndum-Nielsen,K
AU  - Beck,B
AU  - Gyftodimou,J
AU  - Hørlyk,H
AU  - Liljenberg,U
AU  - Petersen,M B
AU  - Pedersen,W
AU  - Petersen,M B
AU  - Sand,A
AU  - Skovby,F
AU  - Stafanger,G
AU  - Zetterqvist,P
AU  - Tommerup,N
TI  - Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms
SN  - 0340-6717
PY  - 1997///0220
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 7
KW  - DNA
KW  - chemistry
KW  - Dinucleotide Repeats
KW  - Elastin
KW  - genetics
KW  - Female
KW  - Gene Deletion
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Karyotyping
KW  - Male
KW  - Polymorphism, Genetic
KW  - Williams Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s004390050311
ER  -