INV (7) AS A RECURRENT ABERRATION IN HUMAN LYMPHOCYTE CULTURESHERVA R.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 95; NO 1; PP. 163-164; BIBL. 5 REF.Article

DAS SYNDROM DES MULIBREY NANISMUS: FALLBERICHT MIT OBDUKTIONSBEFUNDEN BEI EINEM 8 MONATE ALTEN WEIBLICHEN SAEUGLING = LE SYNDROME DU NANISME DE MULIBREY: RAPPORT D'UN CAS ET RESULTATS D'AUTOPSIE CHEZ UN NOURRISSON DE 8 MOIS DE SEXE FEMININFINNI K; HERVA R.1981; KLIN. PAEDIATR.; ISSN 0300-8630; DEU; DA. 1981; VOL. 193; NO 4; PP. 328-330; ABS. ENG; BIBL. 10 REF.Article

TRISOMY 9 P WITH I(9P) AND T(9Q18P)HERVA R; KOIVISTO M.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 237-240; BIBL. 7 REF.Article

DE NOVO TRISOMY 4PTER->Q21.HERVA R; VON WENDT L.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 2; PP. 225-230; BIBL. 16 REF.Article

SERIAL DUPLICATION OF 10(Q21->Q22) IN A MENTALLY RETARDED BOY WITH CONGENITAL MALFORMATIONSKOIVISTO M; HERVA R; LINNA SL et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 224-225; BIBL. 6 REF.Article

THE R(20) SYNDROME.HERVA R; SAARINEN I; LEIKKONEN L et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 281-283; BIBL. 5 REF.Article

INTRA-UTERINE GROWTH AND FATAL FETAL ABNORMALITYKIRKINEN P; JOUPPILA P; HERVA R et al.1983; ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. SUPPLEMENT; ISSN 0300-8835; SWE; DA. 1983; VOL. 62; NO 1; PP. 43-47; BIBL. 18 REF.Article

GASTROINTESTINAL FINDINGS IN ATOPIC CHILDRENKOKKONEN J; SIMILA S; HERVA R et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 3; PP. 249-254; BIBL. 21 REF.Article

MULTICYSTIC KIDNEY: A CLINICAL AND HISTOLOGICAL STUDY OF 13 PATIENTSHEIKKINEN ES; HERVA R; LANNING P et al.1980; ANN. CHIR. GYNAECOL.; FIN; DA. 1980; VOL. 69; NO 1; PP. 15-22; BIBL. 16 REF.Article

THE HYDROLETHALUS SYNDROME: DELINEATION OF A "NEW", LETHAL MALFORMATION SYNDROME BASED ON 28 PATIENTSSALONEN R; HERVA R; NORIO R et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 5; PP. 321-330; BIBL. 7 REF.Article

INHERITED INTERSTITIAL DEL (XP) WITH MINIMAL CLINICAL CONSEQUENCES: WITH A NOTE ON THE LOCATION OF GENES CONTROLLING PHENOTYPIC FEATURESHERVA R; KALUZEWSKI B; DE LA CHAPELLE A et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 1; PP. 43-58; BIBL. 40 REF.Article

Multisynostatic osteodysgenesisHERVA, R; SEPPANEN, U.Pediatric radiology. 1985, Vol 15, Num 1, pp 63-64, issn 0301-0449Article

A DELETION IN CHROMOSOME 22 CAN CAUSE DIGEORGE SYNDROMEDE LA CHAPELLE A; HERVA R; KOIVISTO M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 3; PP. 253-256; BIBL. 20 REF.Article

TRISOMY 10 P PRODUCED BY RECOMBINATION INVOLVING COMPLEX PATERNAL TRANSLOCATION BETWEEN CHROMOSOMES 1 AND 10HERVA R; KORHONEN S; HAAPALA K et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 24; NO 1; PP. 50-53; BIBL. 5 REF.Article

DICENTRIC Y CHROMOSOME ARISING VIA TANDEM TRANSLOCATIONHERVA R; SAARINEN I; SAVIKURKI H et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 2; PP. 115-122; BIBL. 17 REF.Article

Amniotic adhesion malformation syndroms: fetal and placental pathologyHERVA, R; KARKINEN-JAASKELAINEN, M.Teratology (Philadelphia, PA). 1984, Vol 29, Num 1, pp 11-19, issn 0040-3709Article

Hydrolethalus syndromeSALONEN, R; HERVA, R.Journal of medical genetics. 1990, Vol 27, Num 12, pp 756-759, issn 0022-2593, 4 p.Article

Roentgenologic findings of the hydrolethalus syndromeHERVA, R; SEPPANEN, U.Pediatric radiology. 1984, Vol 14, Num 1, pp 41-43, issn 0301-0449Article

PERICENTRIC INVERSIONS OF HUMAN CHROMOSOMES 9 AND 10 = INVERSIONS PERICENTRIQUES DES CHROMOSOMES HUMAINS 9 ET 10DE LA CHAPELLE A; SCHROEDER J; STENSTRAND K et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 26; NO 6; PP. 746-766; BIBL. 2P.Article

A lethal autosomal recessive syndrome of multiple congenital contracturesHERVA, R; LEISTI, J; KIRKINEN, P et al.American journal of medical genetics. 1985, Vol 20, Num 3, pp 431-439, issn 0148-7299Article

Prenatal diagnosis of pleural effusions by ultrasoundJOUPPILA, P; KIRKINEN, P; HERVA, R et al.Journal of clinical ultrasound. 1983, Vol 11, Num 9, pp 516-519, issn 0091-2751Article

IMMUNODEFICIENCY ASSOCIATED WITH A DELETION IN THE SHORT ARM OF THE X-CHROMOSOMENURMI T; UHARI M; LINNA SL et al.1981; CLIN. EXP. IMMUNOL.; ISSN 0009-9104; GBR; DA. 1981; VOL. 45; NO 1; PP. 107-112; BIBL. 24 REF.Article

Lethal arthrogryposis in Finland: a clinico-pathological study of 83 cases during thirteen yearsVUOPALA, K; LEISTI, J; HERVA, R et al.Neuropediatrics. 1994, Vol 25, Num 6, pp 308-315, issn 0174-304XArticle

Risk of malignancy and death in neurofibromatosisPOYHONEN, M; NIEMELA, M. S; HERVA, R et al.Archives of pathology & laboratory medicine (1976). 1997, Vol 121, Num 2, pp 139-143, issn 0363-0153Article

Prenatal detection of hydrolethalus syndromeHARTIKAINEN-SORRI, A.-L; KIRKINEN, P; HERVA, R et al.Prenatal diagnosis. 1983, Vol 3, Num 3, pp 219-224, issn 0197-3851Article