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

Clinical consequences of heterozygosity for autosomal-recessive diseasesVOGEL, F.Clinical genetics. 1984, Vol 25, Num 5, pp 381-415, issn 0009-9163Article

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

Autosomal recessive inheritance : An updated reviewMENSINK, Kara A; HAND, Jennifer L.Pediatric dermatology. 2006, Vol 23, Num 4, pp 404-409, issn 0736-8046, 6 p.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

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

Disturbances in endocannabinoid metabolism causes autosomal recessive neurodegenerationMETZLER, M.Clinical genetics. 2011, Vol 79, Num 3, pp 221-222, issn 0009-9163, 2 p.Article

Peripapillary Retinal Nerve Fiber Layer Thinning in Patients with Autosomal Recessive Cone-Rod DystrophyPASADHIKA, Sirichai; FISHMAN, Gerald A; ALLIKMETS, Rando et al.American journal of ophthalmology. 2009, Vol 148, Num 2, pp 260-265, issn 0002-9394, 6 p.Article

Evidence for autosomal recessive inheritance of progeria (Hutchinson Gilford)TREVAS MACIEL, A.American journal of medical genetics. 1988, Vol 31, Num 3, pp 483-487, issn 0148-7299Article

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

Autosomal dominant inheritance of small kidneysKAPLAN, B. S; MILNER, L. S; JEQUIER, S et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 120-126, issn 0148-7299, 7 p.Article

Ehlers-Danlos syndrome type IV D: an autosomal recessive disorderSULH, H. M. B; STEINMANN, B; RAO, V. H et al.Clinical genetics. 1984, Vol 25, Num 3, pp 278-287, issn 0009-9163Article

Autosomal dominant hypoparathyroidism with intracranial calcification outside the basal gangliaMCLEOD, D. R; HANLEY, D. A; MCARTHUR, R. G et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 32-35, issn 0148-7299, 4 p.Article

Autosomal inheritance of sideroblastic anaemiaAMOS, R. J; MILLER, A. L. C; AMESS, J. A. L et al.Clinical and laboratory haematology. 1988, Vol 10, Num 3, pp 347-353, issn 0141-9854Article

Autosomal recessive inheritance of Nager acrofacial dysostosisCHEMKE, J; MOGILNER, B. M; BEN-ITZHAK, I et al.Journal of medical genetics. 1988, Vol 25, Num 4, pp 230-232, issn 0022-2593Article

Quantitative characters under assortative mating: gametic modelGIMELFARB, A.Theoretical population biology (Print). 1984, Vol 25, Num 3, pp 312-330, issn 0040-5809Article

Mutations in EXPH5 result in autosomal recessive inherited skin fragilityLIU, L; MELLERIO, J. E; MARTINEZ, A. E et al.British journal of dermatology (1951). 2014, Vol 170, Num 1, pp 196-199, issn 0007-0963, 4 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

Autosomal dominant precalcaneal congenital fibrolipomatous hamartomaMEYER, Peter; SOENNICHSEN, Karsten; BUCHENAU, Wolfgang et al.Pediatric dermatology. 2005, Vol 22, Num 4, pp 355-356, issn 0736-8046, 2 p.Article

Hypercoagulability in a patient with Marfan syndromeHUMPHRIES, J. E; STOUFFER, G. A; KELLY, T. E et al.Journal of medical genetics. 1991, Vol 28, Num 5, pp 349-351, issn 0022-2593Article

Autosomal dominant peripheral preretinal depositsGOMOLIN, J. E. S; LUCCHESE, N. J; BRESNICK, G. H et al.Archives of ophthalmology (1960). 1984, Vol 102, Num 1, pp 74-76, issn 0003-9950Article

LA GAMETOGENESE CHEZ LE NEMATODE HERMAPHRODITE CAENORHABDITIS ELEGANS, VARIETE BERGERAC. ETUDE CYTOGENETIQUE DE MUTANTS STERILES NON CONDITIONNELS.MOUNIER N.1978; ; S.L.; DA. 1978; PP. 1-37; H.T. 32; BIBL. 3 P.; (THESE DOCT. SPEC., 3E. CYCLE, SCI. BIOL., BIOL. APPL.; CLAUDE BERNARD-LYON I)Thesis

COLOR MATCHING IN AUTOSOMAL DOMINANT TRITAN DEFECTPOKORNY J; SMITH VC; WENT LN et al.1981; J. OPT. SOC. AM. (1930); ISSN 0030-3941; USA; DA. 1981; VOL. 71; NO 11; PP. 1327-1334; BIBL. 39 REF.Article

AUTOSOMAL HYPOPHOSPHATAEMIC BONE DISEASE RESPONDS TO 1,25-(OH)₂D₃SCRIVER CR; READE T; HALAL F et al.1981; ARCH. DIS. CHILD.; ISSN 0003-9888; GBR; DA. 1981; VOL. 56; NO 3; PP. 203-207; BIBL. 20 REF.Article

AUTOSOMAL RECESSIVE FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHYHARDING AE; THOMAS PK.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1980; VOL. 43; NO 8; PP. 669-678; BIBL. 28 REF.Article