9th international workshop on fragile X syndrome and X-linked mental retardation
Am J Med Genet
.
2000 Oct 23;94(5):345-60.
doi: 10.1002/1096-8628(20001023)94:5<345::aid-ajmg1>3.0.co;2-z.
Authors
J P Fryns
1
,
M Borghgraef
,
T W Brown
,
J Chelly
,
G S Fisch
,
B Hamel
,
A Hanauer
,
D Lacombe
,
L Luo
,
J N MacPherson
,
J L Mandel
,
C Moraine
,
J Mulley
,
D Nelson
,
B Oostra
,
M Partington
,
G J Ramakers
,
H H Ropers
,
F Rousseau
,
C Schwartz
,
P Steinbach
,
C Stoll
,
L Tranebjaerg
,
G Turner
,
H Van Bokhoven
,
A Vianna-Morgante
Affiliation
1
Clinical Genetics Unit/Center for Human Genetics, University Hospital of Leuven, Leuven, Belgium.
PMID:
11050616
DOI:
10.1002/1096-8628(20001023)94:5<345::aid-ajmg1>3.0.co;2-z
No abstract available
Publication types
Congress
MeSH terms
Fragile X Syndrome / genetics*
Fragile X Syndrome / pathology
Genetic Linkage
Humans
Intellectual Disability / genetics*
Intellectual Disability / pathology
X Chromosome / genetics*