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American Journal of Medical Genetics|July 1, 1988
Caudal deficiency sequence in 7q terminal deletionC Schrander-Stumpel, J Schrander, J P Fryns, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
X-linked mental retardation and neurological symptoms: a nosological approachC T Schrander-Stumpel, C J Höweler, J P FrynsDevelopmental 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.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a familyD M Ioan, L Dumitriu, V Belengeariu, et al.Clinical Genetics|August 1, 1992
Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?J P Fryns, P de Cock, H van den BergheGenetic Counseling (Geneva, Switzerland)|November 5, 1999
The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanismK Keymolen, L De Smet, P Bracke, et al.Clinical Genetics|September 1, 1993
Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult heightE Legius, M Mulier, B Van Damme, et al.Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysisT Lukusa, E Smeets, J R Vermeesch, et al.Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Unilateral absence of the trapezius and pectoralis major muscle: a variant of Poland syndromePh Debeer, P Brys, L De Smet, et al.Annales De Genetique|January 1, 1992
Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndromeD M Ioan, C Maximilian, A Kleczkowska, et al.Pageof 89