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Human Genetics|September 22, 1977
Unusually long survival in a case of full triploidy of maternal originJ P Fryns, A van de Kerckhove, P Goddeeris, et al.
Annales De Genetique|January 1, 1994
Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetusJ Van Hove, A Kleczkowska, M De Bruyn, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological featuresA M Wiegers, L M Curfs, H Meijer, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differentiation from a complex cloacal malformation: a case reportI Witters, L Meylaerts, H Peeters, et al.
Annales De Genetique|January 1, 1989
Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotypeJ P Fryns, A Kleczkowska, H Kenis, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Confirmation of a new MR/male pseudohermaphroditism syndrome, Verloes typeC de Die-Smulders, H van Schrojenstein Lantman-De Valk, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Partial trisomy 15q: report of a patient and literature reviewK Chandler, C T Schrander-Stumpel, J Engelen, et al.
Clinical Genetics|October 1, 1986
Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1J P Fryns, A Kleczkowska, M Buttiens, et al.
Annales De Genetique|January 1, 1985
Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newbornsJ P Fryns, A Kleczkowska, C Limbos, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)E Legius, W Daenen, V Vandenbergh, et al.
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