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Annales De Genetique|January 1, 1993
A specific phenotype associated with trisomy 15 mosaicismJ P Fryns, A Kleczkowska, L Lagae, et al.Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Emotional and behavioral profile and child psychiatric diagnosis in the childhood type of myotonic dystrophyE Goossens, J Steyaert, C De Die-Smulders, et al.Annales De Genetique|January 1, 1992
46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficitJ P Fryns, A Kleczkowska, P Decock, et al.Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Multiple congenital anomalies syndrome with multicystic renal dysplasia, postaxial polydactyly and lumbosacral meningocoele. Difficulties in nosological classification and genetic counselingI Witters, Ph Moerman, R Natens, et al.Human Genetics|January 1, 1984
Inactivation pattern of the fragile X in heterozygous carriersJ P Fryns, A Kleczkowska, E Kubień, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Costello syndrome: a postnatal growth retardation syndrome with distinct phenotypeJ P Fryns, A Vogels, J Haegeman, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findingsL A Lizcano-Gil, D Garcia-Cruz, J M Cantu, et al.American Journal of Medical Genetics|April 1, 1992
Cognitive profile in adult, normal intelligent female fragile X carriersJ Steyaert, M Borghgraef, C Gaulthier, et al.European Journal of Pediatrics|August 1, 1992
McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal periodC Schaap, C E de Die-Smulders, R H Kuijten, 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.Pageof 89