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Annales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P SauvageAnnales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D EyerAmerican Journal of Medical Genetics. Part A|September 17, 2004
Do parents and grandparents of patients with achondroplasia have a higher cancer risk?C Stoll, J FeingoldNouvelle Revue Francaise D'Hematologie|January 1, 1982
Y chromosome duplication in chronic myeloid leukemiaC Stoll, F OberlingUltrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 17, 2003
Prenatal diagnosis of dysmorphic syndromes by routine fetal ultrasound examination across EuropeC Stoll, M Clementi, Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Chromosomal region 13q21q31 and heterochrony of developmentC Stoll, V Martel-PetitJournal De Genetique Humaine|June 1, 1975
[Poland's syndrome in a sterile woman]C Stoll, J C SchumacherPageof 33