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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

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

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

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

FREQUENCY OF SISTER CHROMATID EXCHANGES IN BLOOM SYNDROME FIBROBLASTS REDUCED BY COCULTIVATION WITH NORMAL CELLSBARTRAM CR; RUEDIGER HW; PASSARGE E et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 331-334; BIBL. 10 REF.Article

BLOOM'S SYNDROME. V. SURVEILLANCE FOR CANCER IN AFFECTED FAMILIES.GERMAN J; BLOOM D; PASSARGE E et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 3; PP. 162-168; BIBL. 28 REF.Article

FETAL MANIFESTATION OF CHROMOSOMAL DISORDER: PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 5 (5Q33->QTER)PASSARGE E; BARTSCH SANDHOFF M; REHDER H et al.1982; TERATOLOGY; ISSN 0040-3709; USA; DA. 1982; VOL. 25; NO 2; PP. 221-225; BIBL. 15 REF.Article

ZYGOGENETISCHE UND KLINISCHE BEFUNDE BEI VERDACHT AUF TURNER-SYNDROM. ERGEBNISSE EINE 5-JAHRES-STUDIE AN 207 PATIENTEN = CONSTATATIONS CYTOGENETIQUES ET CLINIQUES DANS LA SUSPICION DE SYNDROME DE TURNER. RESULTATS D'UNE ETUDE DE 5 ANS CHEZ 207 MALADESBERGHOFF R; RUDIGER RA; PASSARGE E et al.1976; DTSCHE MED. WSCHR.; DTSCH.; DA. 1976; VOL. 101; NO 14; PP. 532-537; ABS. ANGL.; BIBL. 50 REF.Article

ALPHA 1-ANTITRYPSIN PHENOTYPES IN SEX CHROMOSOME MOSAICISMKUEPPERS F; O'BRIEN P; PASSARGE E et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 3; PP. 263-264; BIBL. 7 REF.Article

PARTIAL TRISOMY 13 PRESUMABLY DUE TO RECOMBINATION IN AN INVERSION HETEROZYGOTE AND BY UNEQUAL CROSSING-OVER.KOSKE WESTPHAL T; PRUSZAK SEEL RE; NISS R et al.1978; ANN. HUM. GENET.; G.B.; DA. 1978; VOL. 41; NO 3; PP. 315-322; H.T. 2; BIBL. 22 REF.Article

Bloom's syndrome. XII: Report from the registry for 1987GERMAN, J; PASSARGE, E.Clinical genetics. 1989, Vol 35, Num 1, pp 57-69, issn 0009-9163Article

Postaxial acrofacial dysostosis syndrome with microcephaly, seizures and profound mental retardationHAUSS-ALBERT, H; PASSARGE, E.American journal of medical genetics. 1988, Vol 31, Num 3, pp 701-703, issn 0148-7299Article

PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOMESCHMIDT A; PASSARGE E; SEEMANOVA E et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 285-286; BIBL. 13 REF.Article

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