TY  - GEN
AU  - Wirtz,M K
AU  - Samples,J R
AU  - Kramer,P L
AU  - Rust,K
AU  - Yount,J
AU  - Acott,T S
AU  - Koler,R D
AU  - Cisler,J
AU  - Jahed,A
AU  - Gorlin,R J
AU  - Godfrey,M
TI  - Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1
SN  - 0148-7299
PY  - 1997///0207
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 15
KW  - Dwarfism
KW  - Eye Abnormalities
KW  - Female
KW  - Fibrillin-1
KW  - Fibrillins
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Humans
KW  - Immunologic Techniques
KW  - Infant
KW  - Male
KW  - Microfilament Proteins
KW  - Microsatellite Repeats
KW  - Middle Aged
KW  - Pedigree
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/(SICI)1096-8628(19961002)65:1<68::AID-AJMG11>3.0.CO;2-P
ER  -