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Two cases of dominant exudative vitreoretinopathyVANHERCK, M; LEYS, A; MISSOTTEN, L et al.Bulletin de la Société belge d'ophtalmologie. 1983, Vol 203, pp 93-97, issn 0081-0746Article

Dominant inheritance of bifid noseANYANE-YEBOA, K; RAIFMAN, M. A; BERANT, M et al.American journal of medical genetics. 1984, Vol 17, Num 3, pp 561-563, issn 0148-7299Article

A second family with autosomal dominant osteosclerosis ― type StanescuDIPIERRI, J. E; GUZMAN, J. D.American journal of medical genetics. 1984, Vol 18, Num 1, pp 13-18, issn 0148-7299Article

Orbital hypotelorism. An isolated autosomal dominant traitJUDISCH, G. F; KRAFT, S. P; BARTLEY, J. A et al.Archives of ophthalmology (1960). 1984, Vol 102, Num 7, pp 995-997, issn 0003-9950Article

Dominant susceptibility to cancer in man = Prédisposition dominante au cancer chez l'hommeHARNDEN, D; MORTEN, J; FEATHERSTONE, T et al.Advances in cancer research. 1984, Vol 41, pp 185-255, issn 0065-230XArticle

Osteogenesis imperfecta type IIA: evidence for dominant inheritanceYOUNG, I. D; THOMPSON, E. M; HALL, C. M et al.Journal of medical genetics. 1987, Vol 24, Num 7, pp 386-389, issn 0022-2593Article

In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg SyndromeCARMIGNAC, Virginie; THEVENON, Julien; RENARD, Marjolijn et al.American journal of human genetics. 2012, Vol 91, Num 5, pp 950-957, issn 0002-9297, 8 p.Article

Severe muscular dystrophy in girlsGARDNER-MEDWIN, D; JOHNSTON, H. M.Journal of the neurological sciences. 1984, Vol 64, Num 1, pp 79-87, issn 0022-510XArticle

INDUCTION DE CARACTERES LETAUX DOMINANTS CHEZ LES MUTANTS RADIOSENSIBLES DE LEVURESSTEPANOVA VP; ZAKHAROV IA.1977; GENETIKA; S.S.S.R.; DA. 1977; VOL. 13; NO 11; PP. 1997-2006; ABS. ANGL.; BIBL. 15 REF.Article

Central areolar pigment epithelial dystrophyHERMSEN, V. M; JUDISCH, G. F.Ophthalmologica (Basel). 1984, Vol 189, Num 1-2, pp 69-72, issn 0030-3755Article

DOMINANT MYOTONIA CONGENITA: PEDIGREE WITH SKIPPING OF ONE GENERATIONBOLTSHAUSER E; MEYER M; METAXAS M et al.1980; J. NEUROL.; DEU; DA. 1980; VOL. 222; NO 4; PP. 235-238; ABS. GER; BIBL. 9 REF.Article

DOMINANTE, INFANTILE MAKULADEGENERATION = DEGENERESCENCE MACULAIRE INFANTILE DOMINANTEHAMMERSTEIN W.1982; KLIN. MONATSBL. AUGENHEILKD.; ISSN 0023-2165; DEU; DA. 1982; VOL. 180; NO 6; PP. 551-552; ABS. ENG; BIBL. 10 REF.Article

DOMINANT INHERITANCE OF INTRACRANIAL BERRY ANEVRYSMEVANS TW; VENNING MC; STRANG FA et al.1981; BR. MED. J.; ISSN 0007-1447; GBR; DA. 1981; VOL. 283; NO 6295; PP. 824-825; BIBL. 5 REF.Article

FURTHER INVESTIGATIONS ON BENIGN MYOPATHY WITH AUTOSOMAL DOMINANT INHERITANCE.ARTS WF; BETHLEM J; VOLKERS WS et al.1978; J. NEUROL.; GERM.; DA. 1978; VOL. 217; NO 3; PP. 201-206; ABS. ALLEM.; BIBL. 1 REF.Article

R75Q Dominant Mutation in GJB2 Gene Silenced by the in Cis Recessive Mutation c.35delGLOSSA, Sandra; CHINETTI, Viviana; CORVINO, Virginia et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 10, pp 2658-2660, issn 1552-4825, 3 p.Article

A new dominantly inherited pure cerebellar ataxia, SCA 30STOREY, E; BAHLO, M; FAHEY, M et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 4, pp 408-411, issn 0022-3050, 4 p.Article

Mate choice, monogamy and mutational loadMCLEAN, K. R; MANNING, J. T.Journal of theoretical biology. 1985, Vol 116, Num 3, pp 369-376, issn 0022-5193Article

Metabolic studies on retinal tissue from a donor with a dominantly inherited chorioretinal degeneration resembling sectoral retinitis pigmentosaHOLLYFIELD, J. G; FREDERICK, J. M; TABOR, G. A et al.Ophthalmology (Rochester, MN). 1984, Vol 91, Num 2, pp 191-196, issn 0161-6420Article

Autosomal dominant paroxysmal kinesigenic choreoathetosis: an electroneurophysiological studyBUSARD, H. L. S. M; RENIER, W. O; GABREELS, F. J. M et al.Clinical neurology and neurosurgery. 1984, Vol 86, Num 4, pp 281-289, issn 0303-8467Article

A dominant mesomelic dysplasia associated with a 1.0-Mb microduplication of HOXD gene cluster at 2q31.1CHO, Tae-Joon; KIM, Ok-Hwa; IN HO CHOI et al.Journal of medical genetics. 2010, Vol 47, Num 9, pp 638-639, issn 0022-2593, 2 p.Article

α-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism : Frequency, Phenotype, and MechanismsIBANEZ, Pablo; LESAGE; AGID, Yves et al.Archives of neurology (Chicago). 2009, Vol 66, Num 1, pp 102-108, issn 0003-9942, 7 p.Article

Minicore myopathy with dominant inheritancePALJARVI, L; KALIMO, H; LANG, H et al.Journal of the neurological sciences. 1987, Vol 77, Num 1, pp 11-22, issn 0022-510XArticle

Distal muscular dystrophy with autosomal recessive inheritanceSCOPPETTA, C; VACCARIO, M. L; CASALI, C et al.Muscle & nerve. 1984, Vol 7, Num 6, pp 478-481, issn 0148-639XArticle

Le syndrome de cancer colique familial: à propos d'une nouvelle famille et revue de la littérature = Familial colonic carcinoma syndrome. Report of a new family and review of literatureMEYER, C; BRAILLON, G; CHASSAGNON, C et al.Lyon médical. 1983, Vol 250, Num 15, pp 143-147, issn 0024-7790Article

Dominant Mutations in RP1L1 Are Responsible for Occult Macular DystrophyAKAHORI, Masakazu; TSUNODA, Kazushige; ITABASHI, Takeshi et al.American journal of human genetics. 2010, Vol 87, Num 3, pp 424-429, issn 0002-9297, 6 p.Article

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