HET GEBRUIK VAN HET H/X DIAGRAM IN DE KLIMATECHNIEK. = THE USE OF THE (H,X) DIAGRAM IN THE AIR CONDITIONING TECHNIQUE = L'EMPLOI DU DIAGRAMME (H,X) DANS LA TECHNIQUE DE CLIMATISATIONMOERMAN P.1977; INGENIEURSBLAD; BELG.; DA. 1977; VOL. 46; NO 8; PP. 209-214; ABS. FR. ANGL. ALLEM.; BIBL. 1 REF.Article

COMPARATIVE STUDY OF THE WATER BALANCE IN THE AERATED ZONES WITH RADIO-ACTIVITE METHODS AND WEIGHABLE LYSIMETER.BOODT M DE; MOERMAN P; BOEVER J DE et al.1968; PUBL.ASSOC.INTERN.HYDROL.SCI.; 1968, VOL. 1, NUM. 0082, P. 63 A 74Miscellaneous

A NEW RADIOGRAPHIC METHOD FOR MEASURING VERTEBRAL ROTATION IN SCOLIOSIS.COETSIER M; VERCAUTEREN M; MOERMAN P et al.1977; ACTA ORTHOP. BELG.; BELG.; DA. 1977; VOL. 43; NO 5; PP. 598-605; ABS. FR. NEERL.; BIBL. 7 REF.Article

PRESSURE DEPENDENT DECAY OF THE ULTRAVIOLET CONTINUUM OF ARGON.MOERMAN P; BOUCIQUE R; MORTIER P et al.1974; PHYS. LETTERS, A; NETHERL.; DA. 1974; VOL. 49; NO 2; PP. 179-180; BIBL. 10 REF.Article

CONGENITAL ATRESIA OF LEFT CORONARY ASTIUMVAN DER HAUWAERT LG; DUMOULIN M; MOERMAN P et al.1982; BR. HEART. J.; ISSN 0007-0769; GBR; DA. 1982; VOL. 48; NO 3; PP. 298-300; BIBL. 7 REF.Article

ASSOCIATION OF MECKEL SYNDROME WITH M-ANISOSPLENIA IN ONE PATIENTMOERMAN P; VERBEKEN E; FRYNS JP et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 3; PP. 143-147; BIBL. 11 REF.Article

CARDIOVASCULAR MALFORMATIONS IN DI GEORGE SYNDROME (CONGENITAL ABSENCE OR HYPOPLASIA OF THE THYMUS)MOERMAN P; GODDEERIS P; LAUWERIJNS J et al.1980; BR. HEART J.; ISSN 0007-0769; GBR; DA. 1980; VOL. 44; NO 4; PP. 452-459; BIBL. 21 REF.Article

The fetal akinesia deformation sequence a fetopathological approachMOERMAN, P; FRYNS, J. P.Genetic counseling. 1990, Vol 1, Num 1, pp 25-33Article

Les maladies rénales polykystiques: morphologie et conseil génétique = Renal polykystic diseases. Morphology and genetic coucnilMOERMAN, P; FRYNS, J.-P.Journal de génétique humaine. 1985, Vol 33, Num 2, pp 157-165, issn 0021-7743Conference Paper

Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome) : A fetopathological studyMOERMAN, P; FRYNS, J. P.Genetic counseling. 1998, Vol 9, Num 1, pp 39-43, issn 1015-8146Conference Paper

THE MECKEL SYNDROME: PATHOLOGICAL AND CYTOGENETIC OBSERVATIONS IN EIGHT CASESMOERMAN P; VERBEKEN E; FRYNS JP et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 240-245; BIBL. 20 REF.Article

Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patientFRYNS, J. P; MOERMAN, P.Journal of medical genetics. 1988, Vol 25, Num 7, pp 498-499, issn 0022-2593Article

Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onsetMOERMAN, P; BARTH, P. G.Virchows Archiv. A, Pathological anatomy and histopathology. 1987, Vol 410, Num 4, pp 339-345, issn 0174-7398Article

SPECTRUM OF CLINICAL AND AUTOPSY FINDINGS IN TRISOMY 18 SYNDROMEMOERMAN P; FRYNS JP; GODDEERIS P et al.1982; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 1; PP. 17-38; ABS. FRE; BIBL. 33 REF.Article

Placental site nodule of the uterine cervixVAN DORPE, J; MOERMAN, P.Histopathology. 1996, Vol 29, Num 4, pp 379-382, issn 0309-0167Article

Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her childMOERMAN, P; FRYNS, J.-P.American journal of medical genetics. 1996, Vol 63, Num 3, pp 479-481, issn 0148-7299Article

A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasiaFRYNS, J. P; MOERMAN, P.Genetic counseling. 1995, Vol 6, Num 1, pp 65-67, issn 1015-8146Article

Diaphragmatic hernia in the Coffin-Siris syndromeDELVAUX, V; MOERMAN, P; FRYNS, J. P et al.Genetic counseling. 1998, Vol 9, Num 1, pp 45-50, issn 1015-8146Conference Paper

Full 69,XXY triploidy and sex-reversal : a further example of true hermaphrodism associated with multiple malformationsPETIT, J; MOERMAN, P; FRYNS, J. P et al.Clinical genetics. 1992, Vol 41, Num 4, pp 175-177, issn 0009-9163Article

Acrofacial dysostosis syndrome type Rodriguez : a new lethal MCA syndromePETIT, P; MOERMAN, P; FRYNS, J.-P et al.American journal of medical genetics. 1992, Vol 42, Num 3, pp 343-345, issn 0148-7299Article

Lobar holoprosencephaly and Xq₂₂ deletionPETIT, P; MOERMAN, P; FRYNS, J. P et al.Genetic counseling. 1991, Vol 2, Num 2, pp 119-121Article

DECIDUAL VASCULOPATHY AND EXTENSIVE PLACENTAL INFARCTION IN A PATIENT WITH REPEATED THROMBOEMBOLIC ACCIDENTS, RECURRENT FETAL LOSS, AND A LUPUS ANTICOAGULANTDE WOLF F; CARRERAS LO; MOERMAN P et al.1982; AM. J. OBSTETR. GYNECOL.; ISSN 0002-9378; USA; DA. 1982; VOL. 142; NO 7; PP. 829-834; BIBL. 22 REF.Article

LIVER NECROSIS IN THE NEW-BORN INFANT: ANALYSIS OF SOME PRECIPITATING FACTORS IN NEONATAL CAREDEVLIEGER H; SNOEYS R; WYNDAELE L et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 2; PP. 113-119; BIBL. 30 REF.Article

Triple negative breast cancer: a study from the point of view of basal CK5/6 and HER-1PINTENS, S; NEVEN, P; DRIJKONINGEN, M et al.Journal of clinical pathology. 2009, Vol 62, Num 7, pp 624-628, issn 0021-9746, 5 p.Article

Intravascular large b-cell lymphoma of the uterus presenting as fever of unknown origin (fuo) and revealed by FDG-PETLANNOO, L; SMETS, S; STEENKISTE, E et al.Acta Clinica Belgica. 2007, Vol 62, Num 3, pp 187-190, issn 0001-5512, 4 p.Article