Results 171 to 180 of about 2,852 (190)
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A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly
Molecular and Cellular Probes, 1994Caroline Hayward, David J H Brock
exaly
Congenital contractural arachnodactyly with unilateral lower limb deficiency
American Journal of Medical Genetics Part A, 1992T R Cole, H E Hughes
exaly
Clinical Features of Congenital Contractural Arachnodactyly
Congenital Anomalies (discontinued), 1993Toshihiko Ogino, Masatoshi Takahara
exaly
FBN2,FBN1,TGFBR1, andTGFBR2 analyses in congenital contractural arachnodactyly
American Journal of Medical Genetics, Part A, 2007Haruya Sakai +2 more
exaly
Cardiovascular findings in congenital contractural arachnodactyly: Report of an affected kindred
American Journal of Medical Genetics Part A, 1984Richard A Anderson +2 more
exaly
The clinical spectrum of congenital contractural arachnodactyly
European Journal of Pediatrics, 1974Chirane Viseskul +2 more
exaly
Congenital contractural arachnodactyly (Beals-Hecht syndrome): a rare connective tissue disorder
Wiener Klinische Wochenschrift, 2013Íngrid Tonhajzerova +1 more
exaly

