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Annales De Genetique|May 26, 1998
Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocationP Petit, K Devriendt, J R Vermeesch, et al.Annales De Genetique|January 1, 1995
Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndromeK Devriendt, K De Mars, P De Cock, et al.Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptomsD Willekens, P De Cock, J P FrynsJournal of Medical Genetics|March 1, 1996
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndromeK Devriendt, L D'Espallier, J P FrynsAmerican Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneJ P Fryns, M D'Hooghe, K DevriendtAnnales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P FrynsClinical Genetics|July 11, 1998
Deletion in chromosome region 22q11 in a child with CHARGE associationK Devriendt, A Swillen, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P FrynsClinical Genetics|August 1, 1992
Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?J P Fryns, P de Cock, H van den BerghePageof 90