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Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Moderate mental retardation without dysmorphic symptoms in intrachromosomal 11p12 duplicationE Goossens, R Cayenberghs, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 13, 2000
On the association profound nerve deafness, semilobar holoprosencephaly, and minor midline developmental anomaliesG Vantrappen, L Feenstra, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 24, 2000
Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndromeI Witters, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 24, 2000
Conductive hearing loss and multiple pre- and supra-auricular skin defects: a variant example of the Branchio-Oculo-Facial syndromeG Vantrappen, L Feenstra, J P FrynsAmerican Journal of Medical Genetics|February 1, 1992
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndromeP Petit, P Moerman, J P FrynsClinical Genetics|April 1, 1992
Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformationsP Petit, P Moerman, J P FrynsJournal De Genetique Humaine|June 1, 1984
[Prune belly syndrome, a secondary urethral functional obstruction due to prostatic hypoplasia]P Moerman, J P Fryns, P GoodeerisGenetic Counseling (Geneva, Switzerland)|August 5, 2010
Preconception careI Witters, A Bogaerts, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomaliesT Lukusa, P Moerman, J P FrynsHuman Genetics|January 1, 1980
Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriersJ P Fryns, H Van den BerghePageof 90