PRAENAETALE DIAGNOSTIK. II. AMNIOZENTESE (FORTS.), CHROMOSOMEN-UNTERSUCHUNG. = DIAGNOSTIC PRENATAL. II. AMNIOCENTESE (SUITE), ETUDE DES CHROMOSOMESSTENGEL RUTKOWSKI S.1978; FORTSCHR. D. MED.; DTSCH.; DA. 1978; VOL. 96; NO 2; PP. 52-55Article

GENETIC RISKS FOR FAMILIAL RECIPROCAL TRANSLOCATIONS WITH SPECIAL EMPHASIS ON THOSE LEADING TO 9P, 10P AND 12P TRISOURIESSTENE J; STENGEL RUTKOWSKI S.1982; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1982; VOL. 46; NO 1; PP. 41-74; BIBL. 4 P.Article

THE DERMATOGLYPHIC PATTERN OF THE TRISOMY 9P SYNDROMERODEWALD A; STENGEL RUTKOWSKI S; ZANKL M et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 6; PP. 405-417; BIBL. 2 P.Article

OBSERVATIONS WITH G BANDING OF HUMAN CHROMOSOMES. REDUCTION OF DYE CONCENTRATION IN SOERENSEN BUFFERED SOLUTIONS IS SUFFICIENT FOR DEMONSTRATING G BANDS = OBSERVATIONS SUR LA COLORATION EN BANDES G DES CHROMOSOMES HUMAINS. LA REDUCTION DE LA TENEUR EN COLORANT DANS LES SOLUTIONS TAMPONNEES DE SOERENSEN EST SUFFISANTE POUR METTRE EN EVIDENCE LES BANDES GWALTHER JU; STENGEL RUTKOWSKI S; MURKEN JD et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 1; PP. 49-51; BIBL. 5REF.Article

PATERNAL AGE AND DOWN'S SYNDROME DATA FROM PRENATAL DIAGNOSES (DFG)STENE J; STENE E; STENGEL RUTKOWSKI S et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 119-124; BIBL. 21 REF.Article

NEW CHROMOSOMAL MALFORMATION SYNDROMES. I. PARTIAL MONOSOMY 8 P. AN ATTEMPT TO ESTABLISH A NEW CHROMOSOME DELETION SYNDROME.RODEWALD A; STENGEL RUTKOWSKI S; SCHULZ P et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 125; NO 1; PP. 45-57; ABS. ALLEM.; BIBL. 13 REF.Article

MOEGLICHKEITEN DER GENETISCHEN BERATUNG ZUR PRAENATALEN DIAGNOSTIK IN DER KINDERAERZTLICHEN PRAXIS = POSSIBILITES DU CONSEIL GENETIQUE POUR LE DIAGNOSTIC PRENATAL EN PRATIQUE PEDIATRIQUEMURKEN JD; STENGEL RUTKOWSKI S; ZAHN V et al.1979; FORTSCHR. D. MED.; DEU; DA. 1979; VOL. 97; NO 34; PP. 1443-1447; BIBL. 6 REF.Article

PRAENATALE DIAGNOSE DER METACHROMATISCHEN LEUKODYSTROPHIE = DIAGNOSTIC PRENATAL DE LA LEUCODYSTROPHIE METACHROMATIQUEHARZER K; ZAHN V; STENGEL RUTKOWSKI S et al.1975; DTSCHE MED. WSCHR.; DTSCH.; DA. 1975; VOL. 100; NO 17; PP. 951-953; ABS. ANGL.; BIBL. 11REF.Article

On methodological issues regarding 47,+21 paternal age dataSTENE, E; STENE, J; STENGEL-RUTKOWSKI, S et al.Human genetics. 1987, Vol 77, Num 4, issn 0340-6717, 317Article

Anthropometric definitions of dysmorphic facial signsSTENGEL-RUTKOWSKI, S; SCHIMANEK, P; WERNHEIMER, A et al.Human genetics. 1984, Vol 67, Num 3, pp 272-295, issn 0340-6717Article

PRAENATALE DIAGNOSE DER GM₂-GANGLIOSIDOSE TYP 2. (SANDHOFF-JATZKEWITZ-KRANKHEIT) = DIAGNOSTIC PRENATAL DE LA GANGLIOSIDOSE GM₂ DE TYPE 2 (MALADIE DE SANDHOFF-JATZKEWITZ)HARZER K; STENGEL RUTKOWSKI S; GLEY EO et al.1975; DTSCHE MED. WSCHR.; DTSCH.; DA. 1975; VOL. 100; NO 3; PP. 106-108; ABS. ANGL.; BIBL. 8 REF.Article

TRANSSEXUALITAET UND H-Y ANTIGEN = TRANSSEXUALISME ET ANTIGENE H-YEICHER W; SPOLJAR M; MURKEN JD et al.1981; FORTSCHR. MED.; ISSN 0015-8178; DEU; DA. 1981; VOL. 99; NO 1-2; PP. 9-12; ABS. ENG; BIBL. 16 REF.Article

NEW CHROMOSOMAL DYSMORPHIC SYNDROMES. III: PARTIAL TRISOMY 3QSTENGEL RUTKOWSKI S; MURKEN JD; PILAR V et al.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 130; NO 2; PP. 111-125; BIBL. 2 P.Article

ROUTINE G-BANDING IN PRENATAL DIAGNOSIS OF CHROMOSOMAL DISORDERSSTENGEL RUTKOWSKI S; WIRTZ A; HAHN B et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 2; PP. 231-234; BIBL. 2 REF.Article

ASPERMIA, ASSOCIATED WITH A PRESUMABLY BALANCED X/AUTOSOMAL TRANSLOCATION. KARYOTYPE 46,Y,T(X;5) (Q28;Q11)STENGEL RUTKOWSKI S; ZANKL H; RODEWALD A et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 1; PP. 97-106; BIBL. 2 P. 1/2Article

NEW CHROMOSOMAL DYSMORPHIC SYNDROME. II. TRISOMY 10P.STENGEL RUTKOWSKI S; MURKEN JD; FRENKENBERGER R et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 126; NO 3; PP. 109-125; ABS. ALLEM.; BIBL. 21 REF.Article

A (3;17) BALANCED TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-2808STENGEL RUTKOWSKI S; WIRTZ A; MURKEN JP et al.1979; CYTOGENET. CELL. GENET; CHE; DA. 1979; VOL. 24; NO 4; PP. 252Article

Juvenile Hyaline Fibromatose = Juvenile hyaline fibromatosisSCHALLER, M; STENGEL-RUTKOWSKI, S; SOLLBERG, S et al.Hautarzt. 1997, Vol 48, Num 4, pp 253-257, issn 0017-8470Article

Childhood hypertrichosis : diagnosis and managementBAUMEISTER, F. A. M; SCHWARZ, H. P; STENGEL-RUTKOWSKI, S et al.Archives of disease in childhood. 1995, Vol 72, Num 5, pp 457-459, issn 0003-9888Article

PRAENATALE DIAGNOSTIK BEI ELTERN MIT EINER BALANCIERTEN CHROMOSOMALEN STRUKTURABERRATION = LE DIAGNOSTIC PRENATAL CHEZ LES PARENTS PRESENTANT UNE ABERRATION CHROMOSOMIQUE BALANCEEWIRTZ A; STENGEL RUTKOWSKI S; STENE J et al.1980; GEBURTSH. FRAUENHEILKDE; DEU; DA. 1980; VOL. 40; NO 7; PP. 575-592; ABS. ENG; BIBL. 19 REF.Article

Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22): case report, review and risk estimatesSTENGEL-RUTKOWSKI, S; WARKOTSCH, A; SCHIMANEK, P et al.Clinical genetics. 1984, Vol 25, Num 6, pp 500-521, issn 0009-9163Article

NEW CHROMOSOMAL DYSMORPHIC SYNDROMES. IV: TRISOMY 12PSTENGEL RUTKOWSKI S; ALBERT A; MURKEN JD et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 136; NO 3; PP. 249-262; BIBL. 33 REF.Article

Ambras syndrome : delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22)BAUMEISTER, F. A. M; EGGER, J; SCHILDHAUER, M. T et al.Clinical genetics. 1993, Vol 44, Num 3, pp 121-128, issn 0009-9163Article

Nonchromosomal dysmorphic syndromes. II: Craniofacial and skeletal anomalies in two similarly affected mentally retarded sibsSCHIEL, W; STENGEL-RUTKOWSKI, S; SHIMANEK, P et al.Dysmorphology and clinical genetics. 1987, Vol 1, Num 3, pp 109-121Article

Formation of supernumerary euchromatic short arm isochromosomes : Parent and cell stage of origin in new cases and review of the literatureEGGERMANN, T; SCHUBERT, R; ENGELS, H et al.Annales de génétique (Paris). 1999, Vol 42, Num 2, pp 75-80, issn 0003-3995Article