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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, La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|April 28, 1983
[School attendance of children with trisomy 21. A 4-year experiment]C Stoll, M P RothGenetic Counseling (Geneva, Switzerland)|January 31, 2006
Chromosomal region 13q21q31 and heterochrony of developmentC Stoll, V Martel-PetitHuman Genetics|January 1, 1980
Partial 4q duplication due to inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of factor XC Stoll, M P RothPageof 30