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Clinical Dysmorphology|August 24, 1999
Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.Developmental Medicine and Child Neurology|October 1, 1996
Cerebellar hypoplasia in a patient with velo-cardio-facial syndromeK Devriendt, M N Thienen, A Swillen, et al.Cytogenetic and Genome Research|September 7, 2006
Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomaliesB Thienpont, M Gewillig, J-P Fryns, et al.American Journal of Medical Genetics. Part A|May 16, 2003
Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third familyPhilippe Debeer, E Pykels, J Lammens, et al.Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.Journal of Medical Genetics|June 27, 1998
Oto-onycho-peroneal syndrome: confirmation of a syndromeK Devriendt, D Stoffelen, R Pfeiffer, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypesP Petit, K Devriendt, M Azou, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
DiGeorge syndrome and unilateral symbrachydactylyK Devriendt, L De Smet, K De Boeck, et al.Pageof 90