SIMPLIFIED METHODS FOR THE MEASUREMENT AND ELECTROPHORETIC DEMONSTRATION OF HYPOXANTHINE-GUANINE PHOSPHORIBOSYL TRANSFERASE = METHODES SIMPLIFIEES DE MESURE ET DE MISE EN EVIDENCE ELECTROPHORETIQUE DE L'HYPOXANTHINE-GUANINE PHOSPHORIBOSYL TRANSFERASEROPERS HH.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 17; NO 1; PP. 69-74; BIBL. 12 REF.Serial Issue

VARIABLE COMPOSITION OF X CHROMOSOMAL MOSAICS. DUE TO ASYNCHRONOUS CELL DIVISION DURING EARLY EMBRYOGENESIS.ROPERS HH; GRIMM T.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 213-215; BIBL. 11 REF.Article

EVIDENCE FOR X-LINKAGE AND NON-INACTIVATION OF STEROID SULPHATASE LOCUS IN WOOD LEMMINGROPERS HH; WIBERG U.1982; NATURE (LOND.); ISSN 0028-0836; GBR; DA. 1982; VOL. 2962; NO 5859; PP. 766-767; BIBL. 23 REF.Article

ON THE INCIDENCE OF UNILATERAL AND BILATERAL COLOUR BLINDNESS IN HETEROZYGOUS FEMALES.FEIG K; ROPERS HH.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 313-323; BIBL. 3 P.Article

CRYPTOCHIDISM AND HYPOGENITALISM IN X-LINKED RECESSIVE ICHTHYOSIS VULGARISTRAUPE H; ROPERS HH.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 206; BIBL. 7 REF.Article

PERIODIC HYPOKALEMIC PARALYSIS TRANSMITTED BY AN UNAFFECTED MALE WITH NEGATIVE FAMILY HISTORY: A DELAYED MUTATION.ROPERS HH; SZLIWOWSKI HB.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 113-116; BIBL. 10 REF.Article

NORMALE AKTIVITAET VON HYPOXANTHIN-GUANIN-PHOSPHORIBOSYLTRANSFERASE BEI PRIMAERER ERWACHSENENGICHT = ACTIVITE NORMALE DE L'HYPOXANTHINE-GUANINE-PHOSPHORIBOXYLTRANSFERASE AU COURS DE LA GOUTTE PRIMITIVE DE L'ADULTEROPERS HH; MERTZ DP.1973; KLIN. WSCHR.; DTSCH.; DA. 1973; VOL. 51; NO 6; PP. 283-284; ABS. ANGL.; BIBL. 11REF.Serial Issue

FLOW CYTOMETRIC CHARACTERIZATION OF A CHINESE HAMSTER X MAN HYBRID CELL LINE RETAINING THE HUMAN Y CHROMOSOMECREMER C; GRAY JW; ROPERS HH et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 3; PP. 262-266; BIBL. 22 REF.Article

ADRENOLEUKODYSTROPHY: DIAGNOSIS AND CARRIER DETECTION BY DETERMINATION OF LONG-CHAIN FATTY ACIDS IN CULTURED FIBROBLASTSTONSHOFF B; LEHNERT W; ROPERS HH et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 1; PP. 25-29; BIBL. 14 REF.Article

ADDISON DISEASE AND CEREBRAL SCLEROSIS IN AN APPARENTLY HETEROZYGONS GIRL: EVIDENCE FOR INACTIVATION OF THE ADRENOLEUKODYSTROPHY LOCUSHEFFUNGS W; HAMEISTER H; ROPERS HH et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 3; PP. 184-188; BIBL. 25 REF.Article

PROGRESSIVE MYOCLONUS EPILEPSY. A VARIANT WITH PROBABLE X LINKED INHERITANCEWIENKER TF; VON REUTERN GM; ROPERS HH et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 1; PP. 83-89; BIBL. 17 REF.Article

ADRENOLEUKODYSTROPHY (SIEMERLING-CREUTZFELDT DISEASE): HETEROZYGOTE WITH TWO CLONAL FIBROBLAST POPULATIONS.ROPERS HH; ZIMMERMANN J; WIENKER T et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 2; PP. 114-118; BIBL. 13 REF.Article

FABRY'S DISEASE: HETEROZYGOTE DETECTION BY HAIR ROOT ANALYSISGRIMM T; WIENKER TF; ROPERS HH et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 3; PP. 329-334; BIBL. 13 REF.Article

FURTHER EVIDENCE FOR THE ASSIGNMENT OF THE STEROID SULFATASE X-LINKED ICHTHYOSIS LOCUS TO THE TELOMER OF XPMUELLER CR; WAHLSTROEM J; ROPERS HH et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 446; BIBL. 4 REF.Article

THE PRESENCE OF ANDROGEN-BINDING RECEPTORS IN GENITAL AND NONGENITAL SKIN FIBROBLASTSHERFERT J; WIENKER TF; ROPERS HH et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 271-273; BIBL. 20 REF.Article

COMPLEMENTATION AFTER FUSION OF SANDHOFF-AND TAY-SACHS FIBROBLASTS = COMPLEMENTATION APRES FUSION DES FIBROBLASTES DE SANDHOFF ET DE TAY-SACHSROPERS HH; GRZESCHIK KH; BUEHLER E et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 117-121; ABS. ALLEM.; BIBL. 13REF.Article

PREFERENTIAL X INACTIVATION IN HUMAN PLACENTA MEMBRANES: IS THE PATERNAL X INACTIVE IN EARLY EMBRYONIC DEVELOPMENT OF FEMALE MAMMALS.ROPERS HH; WOLFF G; HITZEROTH HW et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 265-273; BIBL. 2 P.Article

PRENATAL DIAGNOSIS OF HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: INVESTIGATION OF A CASE AT RISK.WIENKER TF; UTERMANN G; ROPERS HH et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 6; PP. 545-552; BIBL. 20 REF.Article

X-LINKED STEROID SULFATASE: EVIDENCE FOR DIFFERENT GENE-DOSAGE IN MALES AND FEMALESMUELLER CR; MIGL B; TRAUPE H et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 197-199; BIBL. 18 REF.Article

AN XX MALE WITH A SINGLE STS GENE DOSEWIEACKER P; VOICULESCU J; MULLER CR et al.1983; CYTOGENETICS AND CELL GENETICS; ISSN 0301-0171; CHE; DA. 1983; VOL. 35; NO 1; PP. 72-74; BIBL. 14 REF.Article

X-LINKED RECESSIVE ICHTHYOSIS IN THREE SISTERS: EVIDENCE FOR HOMOZYGOSITYMEVORAH B; FRENK E; MUELLER CR et al.1981; BR. J. DERMATOL. (1951); ISSN 0007-0963; GBR; DA. 1981; VOL. 105; NO 6; PP. 711-717; BIBL. 16 REF.Article

ASSIGNMENT OF THE GENE CODING FOR HUMAN CATALASE TO THE SHORT ARM OF CHROMOSOME 11WIEACKER P; MUELLER CR; MAYEROVA A et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 73-77; ABS. FRE; BIBL. 12 REF.Article

TENTATIVE EVIDENCE FOR 3-4 HAEMATOPOETIC STEM CELLS IN MAN.HITZEROTH HW; BENDER K; ROPERS HH et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 35; NO 2; PP. 175-183; BIBL. 13 REF.Article

LEUKODYSTROPHY, SKIN HYPERPIGMENTATION, AND ADRENAL ATROPHY: SIEMERLING-CREUTZFELDT DISEASE. TRANSMISSION THROUGH SEVERAL GENERATIONS IN TWO FAMILIES.ROPERS HH; BURMEISTER P; VON PETRYKOWSKI W et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 4; PP. 547-553; BIBL. 10 REF.Article

LINKAGE STUDIES IN A FAMILY WITH X-LINKED RECESSIVE ICHTHYOSIS EMPLOYING A CLONED DNA SEQUENCE FROM THE DISTAL SHORT ARM OF THE X CHROMOSOMEWIEACKER P; DAVIES KE; MEVORAH B et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 2; PP. 113-116; BIBL. 22 REF.Article