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Journal of Developmental Physiology|December 1, 1991
The diaphragm of the newborn infant: anatomical and ultrasonographic studiesH Devlieger, H Daniels, G Marchal, et al.
American Journal of Medical Genetics|August 28, 1995
Apparently new "anophthalmia-plus" syndrome in sibsJ P Fryns, E Legius, P Moerman, et al.
Pediatric Pathology|May 1, 1994
Hereditary renal adysplasia: new observations and hypothesesP Moerman, J P Fryns, S H Sastrowijoto, et al.
Annales De Genetique|January 1, 1988
The fetal phenotype in 15q2 duplicationJ P Fryns, A Kleczkowska, P Moerman, et al.
Prenatal Diagnosis|August 1, 1994
Prenatal ultrasound diagnosis of rhizomelic chondrodysplasia punctata in a primigravidaS H Sastrowijoto, K Vandenberghe, P Moerman, et al.
Annales De Genetique|January 1, 1990
Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotypeA Kleczkowska, J P Fryns, P Moerman, et al.
Clinical Genetics|October 1, 1983
Aberrant twinning (diprosopus) associated with anencephalyP Moerman, J P Fryns, P Goddeeris, et al.
Human Genetics|December 1, 1988
The pathology of trisomy 13 syndrome. A study of 12 casesP Moerman, J P Fryns, K van der Steen, et al.
American Journal of Medical Genetics|May 1, 1988
Suggestively increased rate of infant death in children of fra(X) positive mothersJ P Fryns, P Moerman, F Gilis, et al.
Clinical Genetics|July 1, 1987
Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3)A Kleczkowska, J P Fryns, P Moerman, et al.
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