TY  - GEN
AU  - Legius,E
AU  - Schollen,E
AU  - Matthijs,G
AU  - Fryns,J P
TI  - Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family
SN  - 1018-4813
PY  - 1998///1110
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Chromosomes, Human, Pair 12
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Genetic Linkage
KW  - Genotype
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Lod Score
KW  - Male
KW  - Noonan Syndrome
KW  - Pedigree
KW  - Skin Abnormalities
KW  - Syndrome
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1038/sj.ejhg.5200150
ER  -