ZUR APPLIKATION HYPERTONER LOESUNGEN UEBER DIE NABELSCHNURGEFAESSE. = SUR L'APPLICATION DE SOLUTIONS HYPERTONIQUES PAR LES VAISSEAUX DU CORDONMUCKE J; VOGTMANN C.1976; ZBL. GYNAEKOL.; DTSCH.; DA. 1976; VOL. 98; NO 1; PP. 34-38; ABS. ANGL.; BIBL. 1 P.Article

AKTUELLE PROBLEME DER THERAPIE BEI HYPERBILIRUBINAEMIE = LES PROBLEMES ACTUELS DU TRAITEMENT DANS L'HYPERBILIRUBINEMIEMUCKE J; BRAUN W.1975; KINDERAERZTL. PRAXIS; DTSCH.; DA. 1975; VOL. 43; NO 8; PP. 337-345; BIBL. 2 P. 1/2Article

MENINGOKOKKEN-MENINGITIS IM NEUGEBORENONALTER = LA MENINGITE A MENINGOCOQUES CHEZ LE NOUVEAU-NEHANDRICK W; MUCKE J.1979; KINDERARZTL. PRAXIS; DDR; DA. 1979; VOL. 47; NO 6; PP. 320-322; ABS. ENG; BIBL. 10 REF.Article

PRASUS DER GENETISCHEN BERATUNG BEI MORBUS DOWN = PRATIQUE DU CONSEIL GENETIQUE DANS LA MALADIE DE DOWNMUCKE J; SANDIG KR; THEILE H et al.1979; DTSCHE GESUNDH.-WES.; DDR; DA. 1979; VOL. 34; NO 2; PP. 70-73; ABS. RUS/ENG; BIBL. 10 REF.Article

ZUR VARIABILITAET DES SMITH-LEMLI-OPITZ-SYNDROMES. BERICHT UEBER ZWEI WEITERE FAELLE. = SUR LA VARIABILITE DU SYNDROME DE SMITH-LEMLI-OPITZ. RAPPORT SUR 2 AUTRES CASMUCKE J; SANDIG KR; BRUCKNER HG et al.1977; PAEDIATR. U. GRENZGEB.; DTSCH.; DA. 1977; VOL. 16; NO 4; PP. 221-228; ABS. ANGL. RUSSE; BIBL. 15 REF.Article

Zur Regulierung des Wassertransportes in pillierten Zuckerrübensaatgut = La régulation du transport de l'eau dans les semences enrobées de betterave sucrière = The regulation of water transport in pelleted sugar-beet seedMÜCKE, J. D.Journal of agronomy and crop science (1986). 1988, Vol 161, Num 2, pp 79-83, issn 0931-2250Article

UEBER INFEKTION DURCH B-STREPTOKOKKEN BEI NEUGEBORENEN = SUR L'INFECTION PAR LES BETA -STREPTOCOQUES CHEZ LE NOUVEAU-NEHANDRICK W; MUCKE J; SCHEERSCHMIDT G et al.1978; PAEDIATR. U. PAEDOL.; AUT; DA. 1978; VOL. 13; NO 4; PP. 377-384; ABS. ENG; BIBL. 67 REF.Article

Augensymptome bei konnatalem Lymphödem = Signes oculaires du lymphœdème congénital = Ophtalmic symptoms in congenital lymphedemaGORNIG, H; MÜCKE, J.Ophthalmologica (Basel). 1985, Vol 191, Num 3, pp 133-138, issn 0030-3755Article

Variability in the proteus syndrome: report of an affected child with progressive lipomatosisMUCKE, J; WILLGERODT, H; KUNZEL, R et al.European journal of pediatrics. 1985, Vol 143, Num 4, pp 320-323, issn 0340-6199Article

MIDAS syndrome (microphthalmia, dermal aplasia and sclerocornea): an autonomous entity with linear skin defects within the spectrum of focal hypoplasiasMÜCKE, J; HOEPFFNER, W; THAMM, B et al.EJD. European journal of dermatology. 1995, Vol 5, Num 3, pp 197-203, issn 1167-1122Article

Das 13q ― Syndrom ― Die partielle Monosomie für den distalen Abschnitt des langen Armes des Chromosom 13 = Le syndrome 13q ― La monosomie partielle pour la partie distale du bras long du chromosome 13MÜCKE, J; SANDIG, K.-R; TRAUTMANN, U et al.Klinische Pädiatrie. 1983, Vol 195, Num 5, pp 361-364, issn 0300-8630Article

Early onset lymphoedema, recessive form ― a new form of genetic lymphoedema syndromeMÜCKE, J; HOEPFFNER, W; SCHEERCHMIDT, G et al.European journal of pediatrics. 1986, Vol 145, Num 3, pp 195-198, issn 0340-6199Article

Zur Reaktivität von 3-Amino-4-imino-2-thioxo-1,2,3,4-tetrahydro-chinazolin und 3-Amino-4-imino-2-selenoxo-1,2,3,4-tetrahydro-chinazolin = Reactivity of 3-amino-4-imino-2-thioxo-1,2,3,4-tetrahydro-quinazolines and 3-amino-4-imino-2-selenoxo-1,2,3,4-tetrahydro-quinazolinesPFEIFFER, W. D; PAZDERA, P; HETZHEIM, A et al.Pharmazie. 1995, Vol 50, Num 1, pp 21-25, issn 0031-7144Article

MITOTIC BEHAVIOR OF EXPANDED CGG REPEATS STUDIED ON CULTURED CELLS : FURTHER EVIDENCE FOR METHYLATION-MEDIATED TRIPLET REPEAT STABILITY IN FRAGILE X S YNDROMEGLASER, D; WOHRLE, D; SALAT, U et al.American journal of medical genetics. 1999, Vol 84, Num 3, pp 226-228, issn 0148-7299, 3 p.Article

X-linked dominant Charcot-Marie-tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal XqGAL, A; MÜCKE, J; THEILE, H et al.Human genetics. 1985, Vol 70, Num 1, pp 38-42, issn 0340-6717Article

Unusual mutations in high functioning fragile X males : apparent instability of expanded unmethylated CGG repeatsWÖHRLE, D; SALAT, U; GLÄSER, D et al.Journal of medical genetics. 1998, Vol 35, Num 2, pp 103-111, issn 0022-2593Article

Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeSCHULZ, A. L; ALBRECHT, B; KÖNIG, R et al.Clinical genetics. 2008, Vol 73, Num 1, pp 62-70, issn 0009-9163, 9 p.Article