INTERSTITIAL DELETION OF 13Q ASSOCIATED WITH RETINOBLASTOMA AND CONGENITAL MALFORMATIONSPETIT P; FRYNS JP.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 2; PP. 106-107; ABS. FRE; BIBL. 9 REF.Article

RING CHROMOSOME 22 IN A MENTALLY RETARDED CHILD AND MOSAIC 45,XX,-15, -22,+T(15; 22) (P11; Q11)/46, XX, R(22)/46, XX KAROTYPE IN THE MOTHERFRYNS JP; VANDEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 213-216; BIBL. 5 REF.Article

TRANSLOCATION 46.X.T(Y.14) (Q122;Q111) IN A CASE OF STERILITY IN THE MALEPETIT P; UNGLIK A; FRYNS JP et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 63-64; ABS. FRE; BIBL. 6 REF.Article

THE COHEN SYNDROMEFRYNS JP; VAN DEN BERGHE H.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 4; PP. 449-453; ABS. FRE; BIBL. 6 REF.Article

SEX-LINKED RECESSIVE INHERITANCE IN CHARCOT-MARIE-TOOTH DISEASE WITH PARTIAL CLINICAL MANIFESTATIONS IN FEMALE CARRIERSFRYNS JP; VAN DEN BERGHE H.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 55; NO 3; PP. 413-415; BIBL. 7 REF.Article

CORNEAL CLOUDING, SUBVALVULAR AORTIC STENOSIS, AND MIDFACIAL HYPOPLASIA ASSOCIATED WITH MENTAL DEFICIENCY AND GROWTH RETARDATION, A NEW SYNDROME.FRYNS JP; VAN DEN BERGHE H.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 131; NO 3; PP. 179-183; BIBL. 10 REF.Article

TRISOMY 18 SYNDROME.FRYNS JP; VAN DEN BERGHE H.1978; ACTA PAEDIATR. BELG.; BEL; DA. 1978; VOL. 31; SUPPL. 7; (8 P.); BIBL. 5 REF.Serial Issue

OCULAR SYMPTOMS IN CORNELIA DE LANGE SYNDROME.EVENS L; VINKEN L; FRYNS JP et al.1977; BULL. SOC. BELGE OPHTALMOL.; BELG.; DA. 1977; VOL. 175; PP. 34-43; ABS. NEERL. FR. ALLEM.; BIBL. 22 REF.Article

PRE AND POSTNATAL GROWTH RETARDATION WITH SEVERE MENTAL RETARDATION, ACRAL LIMB DEFICIENCIES AND OCULAR ANOMALIES. A NEW SYNDROME OF INHERITED INTRAUTERINE DWARFISM.FRYNS JP; VAN DEN BERGHE H.1977; ACTA PEDIATR. BELG.; BELG.; DA. 1977; VOL. 30; NO 4; PP. 227-232; BIBL. 29 REF.Article

MULTIPLE DIFFUSE HEMANGIOMATOSIS. CASE REPORT AND REVIEW OF THE LITERATURE = HEMANGIOMATOSE DIFFUSE MULTIPLE. OBSERVATION D'UN CAS ET REVUE DE LA LITTERATUREFRYNS JP; EGGERMONT E; EECKELS R et al.1974; Z. KINDERHEILKDE; DTSCH.; DA. 1974; VOL. 117; NO 2; PP. 115-119; BIBL. 19REF.Article

PARACENTRIC INVERSION IN MAN: PERSONAL EXPERIENCE AND REVIEW OF THE LITERATUREFRYNS JP; VAN DEN BERGHE H.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 3; PP. 413-416; BIBL. 7 REF.Article

SILVER STAINING OF THE SUPERNUMERARY CHROMOSOME IN THE CAT-EYE SYNDROMEPETIT P; GODART S; FRYNS JP et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 114-116; ABS. FRE; BIBL. 10 REF.Article

13 TRISOMY SYNDROMEFRYNS JP; VAN DEN BERGHE H.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; SUPPL. 14; 4 P.; BIBL. 3 REF.Serial Issue

CONGENITAL SCALP DEFECTS ASSOCIATED WITH POSTAXIAL POLYDACTYLYFRYNS JP; VAN DEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 217-219; BIBL. 3 REF.Article

LANGER TYPE OF MESOMELIC DWARFISM AS THE POSSIBLE HOMOZYGOUS EXPRESSION OF DYSCHONDROSTEOSISFRYNS JP; VAN DEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 21-27; BIBL. 16 REF.Article

POSSIBLE EXCESS OF MENTAL HANDICAP AND CONGENITAL MALFORMATIONS IN AUTOSOMAL RECIPROCAL TRANSLOCATIONSFRYNS JP; VAN DEN BERGHE H.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 125-127; ABS. FRE; BIBL. 11 REF.Article

Y TO X TRANSLOCATION IN MAN.VAN DER BERGHE H; PETIT P; FRYNS JP et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 2; PP. 129-141; BIBL. 2 REF.Article

UNUSUAL 13/13 TRANSLOCATION AND 13 TRISOMY PHENOTYPEFRYNS JP; KLECZKOWSKA A; KUBIEN E et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 113-115; ABS. FRE; BIBL. 5 REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME NUMBER 9: A CLINICAL ENTITYFRYNS JP; VAN DEN BERGHE H.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; SUPPL.; 8 P.; BIBL. 5 REF.Article

SMALL ACCESSORY CHROMOSOMES (SAC) AND THEIR GENOTYPE: PHENOTYPE CORRELATIONFRYNS JP; KLECZKOWSKA A; VAN DEN BERGHE H et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 215-232; ABS. FRE; BIBL. 57 REF.Article

THE ELFIN FACE SYNDROME AND THE SHORT ARM OF CHROMOSOME 15FRYNS JP; VAN DER HAUWAERT LG; VAN DEN BERGHE H et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 181-182; ABS. FRE; BIBL. 11 REF.Article

DISTAL 10P DELETION SYNDROMEFRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 189-190; ABS. FRE; BIBL. 7 REF.Article

MOSAIC SUPERNUMERARY SMALL RING CHROMOSOMEFRYNS JP; VAN HERCK G; VAN DEN BERGHE H et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 2; PP. 151-154; ABS. FRE; BIBL. 6 REF.Article

THE 4P-SYNDROME IN A 24-YEAR-OLD FEMALEFRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 2; PP. 110-111; ABS. FRE; BIBL. 5 REF.Article

PARTIAL TRISOMY 13 WITH PHENOTYPE OF PATAU SYNDROME DUE TO MATERNAL RECIPROCAL TRANSLOCATION T(6;13)(Q25;Q13)PETIT P; FRYNS JP; VAN DEN BERGHE H et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 1; PP. 57-59; ABS. FRE; BIBL. 13 REF.Article