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Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Pre- and postnatal growth retardation--severe mental retardation--acral limb deficiencies with poorly keratinized nails. Another example of a distinct syndrome of inherited intrauterine dwarfism?J Cartwright, M Nelson, J P FrynsAmerican Journal of Medical Genetics|May 1, 1988
The concurrence of Klinefelter syndrome and fragile X syndromeJ P Fryns, H Van den BergheClinical Genetics|July 11, 1998
Deletion in chromosome region 22q11 in a child with CHARGE associationK Devriendt, A Swillen, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Smith-Lemli-Opitz syndrome: the changing phenotype with ageC de Die-Smulders, J P FrynsAmerican Journal of Medical Genetics|December 26, 2001
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter)M Syrrou, M Borghgraef, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Costello syndrome: the natural history of a true postnatal growth retardation syndromeS Umans, P Decock, J P FrynsAnnales De Genetique|January 1, 1980
Partial duplication of the long arm of chromosome 4J P Fryns, H van den BergheAmerican Journal of Medical Genetics|July 15, 1994
Apparently enhanced visual information processing in female fragile X carriers: preliminary findingsJ Steyaert, M Borghgraef, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 26, 2009
A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphismH Peeters, J Vermeesch, J P FrynsPageof 89