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

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

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

Dominant Mutation of CCDC78 in a Unique Congenital Myopathy with Prominent Internal Nuclei and Atypical CoresMAJCZENKO, Karen; DAVIDSON, Ann E; LI, Jun Z et al.American journal of human genetics. 2012, Vol 91, Num 2, pp 365-371, issn 0002-9297, 7 p.Article

Evidence for Autosomal Dominant Inheritance of Ablepharon―Macrostomia SyndromeROHENA, Luis; KUEHN, Devon; MARCHEGIANI, Shannon et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 4, pp 850-854, issn 1552-4825, 5 p.Article

A novel mutation of COL2A1 resulting in dominantly inherited rhegmatogenous retinal detachmentRICHARDS, Allan J; MEREDITH, Sarah; POULSON, Arabella et al.Investigative ophthalmology & visual science. 2005, Vol 46, Num 2, pp 663-668, issn 0146-0404, 6 p.Article

Sample-size guidelines for linkage analysis of a dominant locus for a quantitative trait by the method of lod scoresBOEHNKE, M.American journal of human genetics. 1990, Vol 47, Num 2, pp 218-227, issn 0002-9297, 10 p.Article

Rapports et communications. II: Maladies dominantes à expressivité variable/13èmes Journées européennes de conseil génétique, Athènes, Grèce, 2-5 octobre 1987 = Reports and communications. II: Dominant disease with variable expressivity/13th european days of genetic counseling, Athens, Greece, 2-5 October 1987ROBERT, J. M.Journal de génétique humaine. 1988, Vol 26, Num 3, pp 141-274, issn 0021-7743Conference Proceedings

Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome?AL-AWADI, S. A; NAGUIB, K. K; FARAG, T. I et al.Journal of medical genetics. 1987, Vol 24, Num 6, pp 369-372, issn 0022-2593Article

Transmission héréditaire et manifestation des gènes dominants à pénétrance variable: aspects évolutifsRUVINSKIJ, A. O.Genetika. 1987, Vol 23, Num 6, pp 1038-1049, issn 0016-6758Article

Dominantly inherited craniodiaphyseal dysplasia: a new craniotubular dysplasiaSCHAEFER, B; STEIN, S; OSHMAN, D et al.Clinical genetics. 1986, Vol 30, Num 5, pp 381-391, issn 0009-9163Article