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Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.
https://arctichealth.org/en/permalink/ahliterature194650
Source
J Med Genet. 2001 Mar;38(3):198-202
Publication Type
Article
Date
Mar-2001
More detail
Author
F K Wong
H. Koillinen
J. Rautio
B T Teh
R. Ranta
A. Karsten
O. Larson
S. Linder-Aronson
J. Huggare
C. Larsson
J. Kere
Source
J Med Genet. 2001 Mar;38(3):198-202
Date
Mar-2001
Language
English
Publication Type
Article
Keywords
Chromosomes, Human, Pair 1 - genetics
Chromosomes, Human, Pair 17 - genetics
Cleft Lip - genetics
Family Health
Female
Finland
Genetic Heterogeneity
Genetic Linkage
Genotype
Humans
Lip - abnormalities
Lod Score
Male
Microsatellite Repeats
Pedigree
Phenotype
Syndrome
PubMed ID
11303516
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