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CONGENITAL MALFORMATION SYNDROMES AND EVALUATION OF AMNIOTIC FLUID ALPHA ₁-FETOPROTEINBURCK U; HELD KR; KITSCHKE HJ et al.1981; TEROTOLOGY; ISSN 0040-3709; USA; DA. 1981; VOL. 24; NO 2; PP. 125-130; BIBL. 12 REF.Article

DAS XX-MALE SYNDROM AUS ANDROLOGISCHER SICHT = SYNDROME XX MALEPUSCH H; HELD KR; SCHIRREN C et al.1980; ANDROLOGIA; DEU; DA. 1980; VOL. 12; NO 3; PP. 219-224; ABS. ENG; BIBL. 8 REF.Article

INTERMITTIERENDE VERZWEIGTKETTIGE KETOACIDURIE BEI KETOTISCHER HYPOGLYKAEMIE: UNTERSUCHUNGEN ZUR LOKALISATION DES BIOCHEMISCHEN DEFEKTS = UNE CETO-ACIDURIE INTERMITTENTE DANS L'HYPOGLYCEMIE CETOSIQUE: LES RECHERCHES POUR LA LOCALISATION DU DEFAUT BIOCHIMIQUEHELD KR; STERNOWSKY HJ; SINGH S et al.1976; MONATSSCHR. KINDERHEILKDE; DTSCH.; DA. 1976; VOL. 124; NO 2; PP. 59-65; ABS. ANGL.; BIBL. 15 REF.Article

ULTRASTRUCTURAL PATHOLOGY OF SKIN BIOPSY AND FIBROBLAST ENZYME STUDIES IN A CASE OF GM₂-GANGLIOSIDOSIS WITH DEFICIENT HEXOSAMINIDASE A AND THERMOLABILE HEXOSAMINIDASE BBUCK U; HARZER K; GOEBEL HH et al.1980; NEUROPAEDIATRIE; DEU; DA. 1980; VOL. 11; NO 2; PP. 161-175; ABS. GER; BIBL. 28 REF.Article