CYSTISCHE FIBROSE. GENETIK UND ERBBERATUNG. = LA MUCOVISCIDOSE: GENETIQUE ET CONSEIL GENETIQUEPASSARGE E.1978; MONATSSCHR. KINDER HEILKDE; DTSCH.; DA. 1978; VOL. 126; NO 4; PP. 172-173; BIBL. 4 REF.Article

LEOPARD SYNDROME = SYNDROME DU LEOPARDPASSARGE E.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 468-469Article

MARDEN-WALKER SYNDROME. = SYNDROME DE MARDEN-WALKERPASSARGE E.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 470-471Article

EMIL HEITZ AND THE CONCEPT OF HETEROCHROMATIN: LONGITUDINAL CHROMOSOME DIFFERENTIATION WAS RECOGNIZED FIFTY YEARS AGOPASSARGE E.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 2; PP. 106-115; BIBL. 30 REF.Article

GENETIC HETEROGENEITY RECOGNIZED BY WAARDENBURG IN 1935PASSARGE E.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 23; NO 3; PP. 300-301; BIBL. 4 REF.Article

FAMILIAL OCCURRENCE OF A SHORT RIB SYNDROME WITH HYDROPS FETALIS BUT WITHOUT POLYDACTYLYPASSARGE E.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 403-405; BIBL. 1 REF.Article

INDIKATIONEN ZUR CHROMOSOMENANALYSE. = INDICATIONS POUR DES ANALYSES CHROMOSOMIQUES.PASSARGE E.1978; INTERNIST; DEU; DA. 1978; VOL. 19; NO 8; PP. 445-451; BIBL. 18 REF.Article

SYNDROME OF POLYDACTYLY, MICROMELIA, GENITAL HYPOPLASIA AND RESPIRATORY DISTRESS (MAJEWSKI SYNDROME). = SYNDROME ASSOCIANT POLYDACTYLIE, MICROMELIE, HYPOPLASIE GENITALE ET DETRESSE RESPIRATOIRE OU SYNDROME DE MAJEWSKIPASSARGE E.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 464-465Article

GENETISCH BEDINGTE NIERENKRANKHEITEN. = NEPHROPATHIES D'ORIGINE GENETIQUEPASSARGE E.1978; THERAPIEWOCHE; DTSCH.; DA. 1978; VOL. 28; NO 17; PP. 3476-3480 (3P.); BIBL. 7 REF.Article

SPONTANEOUS CHROMOSOMAL INSTABILITY = INSTABILITE CHROMOSOMIQUE SPONTANEEPASSARGE E.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 16; NO 1-2; PP. 151-177 (8 P.); BIBL. 11 REF.Serial Issue

MULTIPLE Y-CHROMOSOMAL ABERRATIONS IN A PATIENT WITH MIXED GONADAL DYSGENESIS OF XO/XY TYPESCHMIDT A; PASSARGE E.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 445Article

CONGENITAL OSTEOGENESIS IMPERFECTA IN THREE SIBSBRAGA S; PASSARGE E.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 441-443; BIBL. 9 REF.Article

BRIEF CLINICAL REPORT: GENETIC HETEROGENEITY OF XY GONADAL DYSGENESIS (SWYER SYNDROME): H-Y ANTIGEN-NEGATIVE XY GONADAL DYSGENESIS ASSOCIATED WITH INFLAMMATORY BOWEL DISEASEPASSARGE E; WOLF U.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 4; PP. 437-441; BIBL. 12 REF.Article

A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6 (p11.2q15)PASSARGE, E.Cytogenetics and cell genetics. 2000, Vol 91, Num 1-4, pp 192-198, issn 0301-0171Article

THE DELIVERY OF GENETIC COUNSELING SERVICES IN EUROPEPASSARGE E; VOGEL F.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 1; PP. 1-5; BIBL. 9 REF.Article

AUTOSOMAL RECESSIVE HYPOHIDROTIC ECTODERMAL DYSPLASIA WITH SUBCLINICAL MANIFESTATION IN THE HETEROZYGOTE.PASSARGE E; FRIES E.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 36; PP. 95-100; BIBL. 7 REF.Article

SPORADIC TRANSLOCATION, INVERSION, AND MARKER CHROMOSOME IN PRENATAL DIAGNOSISSCHMIDT A; PASSARGE E.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 445Article

UV-LIGHT INDUCED SISTER CHROMATID EXCHANGES IN XERODERMA PIGMENTOSUM LYMPHOCYTES.SCHONWALD AD; PASSARGE E.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 2; PP. 213-218; BIBL. 16 REF.Article

DERIVATIVE CHROMOSOMAL STRUCTURES FROM A RING CHROMOSOME 4 = STRUCTURES CHROMOSOMIQUES DERIVEES D'UN CHROMOSOME 4 EN ANNEAUNISS R; PASSARGE E.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 1; PP. 9-23; ABS. ANGL.; BIBL. 1 P.Article

Bloom's syndrome : the german experiencePASSARGE, E.Annales de génétique (Paris). 1991, Vol 34, Num 3-4, pp 179-197, issn 0003-3995Article

SYMPHALANGIE-STAPESFIXATION-SYNDROM: EINE AUTOSOMAL DOMINANT ERBLICHE ERKRANKUNG, DIE KLINISCH EINE "JUVENILE OTOSKLEROSE" IMITIEREN KANN = SYNDROME SYMPHALANGIE-FIXATION DE L'ETRIER: UNE MALADIE HEREDITAIRE A TRANSMISSION AUTOSOMIQUE DOMINANTE, QUI CLINIQUEMENT PEUT IMITER UNE "OTOSCLEROSE JUVENILE"MEINECKE P; PASSARGE E.1978; DTSCHE MED. WSCHR.; DEU; DA. 1978; VOL. 103; NO 42; PP. 1660-1665; ABS. ENG; BIBL. 11 REF.Article

TRISOMY & RESTRICTED TO CULTURED FIBROBLASTS.NISS R; PASSARGE E.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 3; PP. 229-234; BIBL. 27 REF.Article

³H-THYMIDINE INCORPORATION AT THE END OF THE S PHASE IN CULTURED HUMAN LYMPHOCYTES = INCORPORATION DE LA THYMIDINE-H³ DANS LES LYMPHOCYTES HUMAINS EN CULTURE A LA FIN DE LA PHASE SBERGHOFF D; PASSARGE E.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 2; PP. 141-144; ABS. ALLEM.; BIBL. 10REF.Article

ZYTOGENETISCHER PATERNITAETSNACHWEIS BEI VATER-TACHTER-INZEST. = PREUVE CYTOGENETIQUE DE PARTERNITE DANS L'INCESTE PERE-FILLEKOSKE WESTPHAL T; PASSARGE E.1977; DTSCHE MED. WOCHR.; DTSCH.; DA. 1977; VOL. 102; NO 27; PP. 999-1000; ABS. ANGL.; BIBL. 6 REF.Article

OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION = SYNDROME OCULOCEREBRAL AVEC HYPOPIGMENTATIONPASSARGE E; FUCHS MECKE S.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 466-467Article