DIE ZLAMBACH-SCHICHTEN (ALPINE OBERTRIAS) UNTER BESONDERER BERUECKSICHTIGUNG DER OSTRAKODEN, 2): ZUR STRATIGRAPHIE UND FAZIES DER ZLAMBACH-SCHICHTEN. = COUCHES DE ZLAMBACH (TRIAS SUP. ALPIN) ET PLUS PARTICULIEREMENT ETUDES DES OSTRACODES, 2): STRATIGRAPHIEBOLZ H.1974; SENCKENBERG. LETHAEA; DEU; 1974, VOL. 55, NUM. 0001-0005, P. 325 A 361Serial Issue

LATE TRIASSIC BAIRDIIDAE AND HEALDIIDAE.BOLZ H.1971; BULL. CENTRES RECH. EXPLOR.-PRODUCT. ELF-AQUITAINE; FRA; 1971, VOL. 5Miscellaneous

DER "BAIRDOPPILATE" VERSCHLUSS UND SKULPTUR-UNTERSCHIEDE BEI BAIRDIEN (OSTRAC.) DER ALPINEN OBERTRIAS. (LA PARENTE "BAIRDOPILATE" ET LA DISTINCTION DES SCULPTURES CHEZ LES BAIRDIAE -OSTRACODA- DU TRIAS SUP. ALPIN).BOLZ H.1969; SENCKENBERG. LETHAEA; DEU; 1969(12), VOL. 50, P. 411 A 431Miscellaneous

CLASTIC ACCUMULATION OF SULPHATE EVAPORITES IN DEEP WATER.SCHLAGER W; BOLZ H.1977; J. SEDIMENT. PETROL.; U.S.A.; DA. 1977; VOL. 47; NO 2; PP. 600-609; BIBL. 1 P. 1/2; 11 ILL.Article

On the evaluation of matrix functions given by power seriesBOLZ, H; NIETHAMMER, W.SIAM journal on matrix analysis and applications. 1988, Vol 9, Num 2, pp 202-209, issn 0895-4798Article

Eighteen novel mutations in patients with Lesch-Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiencyWILLERS, I; BOLZ, H; WEHNERT, M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 7, pp 845-846, issn 0141-8955Article

Combinatorial preparation of solid-state materials by injection mouldingREN, S; KOCHANEK, W; BOLZ, H et al.Journal of the European Ceramic Society. 2008, Vol 28, Num 16, pp 3005-3010, issn 0955-2219, 6 p.Article

Phenotypic variability in rippling muscle diseaseVORGERD, M; BOLZ, H; PATZOLD, T et al.Neurology. 1999, Vol 52, Num 7, pp 1453-1459, issn 0028-3878Article

Electrochemical investigation of the nanostructured composite (W,Ga)BOLZ, H; SCHWITZGEBEL, G.Berichte der Bunsen-Gesellschaft. 1997, Vol 101, Num 11, pp 1746-1749, issn 0940-483XConference Paper

DOUBLE HOMOZYGOSITY FOR MUTATIONS OF AGL AND SCN9A MIMICKING NEURO-HEPATOPATHY SYNDROMEEBERMANN, I; ELSAYED, S. M; ABDEL-GHAFFAR, T. Y et al.Neurology. 2008, Vol 70, Num 24, pp 2343-2344, issn 0028-3878, 2 p., 1Article

Characterisation of severe rod―cone dystrophy in a consanguineous family with a splice site mutation in the MERTK geneCHARBEL ISSA, P; BOLZ, H. J; EBERMANN, I et al.British journal of ophthalmology. 2009, Vol 93, Num 7, pp 920-925, issn 0007-1161, 6 p.Article

GPR98 mutations cause Usher syndrome type 2 in malesEBERMANN, I; WIESEN, M. H. J; ZRENNER, E et al.Journal of medical genetics. 2009, Vol 46, Num 4, pp 277-280, issn 0022-2593, 4 p.Article

A novel DFNB 1 deletion allele supports the existence of a distant cis -regulatory region that controls GJB2 and GJB6 expressionWILCH, E; AZAIEZ, H; HOEFSLOO, L et al.Clinical genetics. 2010, Vol 78, Num 3, pp 267-274, issn 0009-9163, 8 p.Article