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

GENETIC STUDIES OF HUMAN ACIDIC SALIVARY PROTEIN (PA).FRIEDMAN RD; MERRITT AD; RIVAS ML et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 3; PP. 292-303; BIBL. 12 REF.Article

AUTOSOMAL RECESSIVE SENSORINEURAL DEAFNESS: A COMPARISON OF TWO KINDREDS = SURDITE NEUROSENSORIELLE AUTOSOMIQUE RECESSIVE: UNE COMPARAISON DE DEUXFAMILLESMCLEOD AC; SWEENEY A; MCCONNELL FE et al.1973; SOUTH. MED. J.; U.S.A.; DA. 1973; VOL. 66; NO 1; PP. 141-152; BIBL. 19REF.Serial Issue

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

LIPID DEFICIENCIES, LEUKOCYTOSIS, BRITTLE SKIN. A LETHAL SYNDROME CAUSED BY A RECESSIVE MUTATION, EDEMATOUS (OED), IN THE MOUSE = DEFICIENCES LIPIDIQUES, LEUCOCYTOSE, PEAU FRAGILE. UN SYNDROME LETAL CAUSE PAR UNE MUTATION RECESSIVE, EDEMATOUS (OED), CHEZ LA SOURISSCHIFFMAN MB; SANTORINEOU ML; LEWIS SE et al.1975; GENETICS; U.S.A.; DA. 1975; VOL. 81; NO 3; PP. 525-536; BIBL. 1 P.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

THE INHERITANCE OF MELANOTIC LARVA IN CULEX PIPIENS L.TADANO T; BARR AR.1975; J. MED. ENTOMOL.; HAWAII; DA. 1975; VOL. 11; NO 6; PP. 751-753; BIBL. 6REF.Article

HETEROGENIC MONOZYGOCITY: EVIDENCE FOR THE TRANSMISSION OF HALF CHROMATID MUTATIONS IN HUMANS.CANTU JM.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 2; PP. 190-191; BIBL. 9 REF.Article

BENIGN MYOPATHY, WITH AUTOSOMAL DOMINANT INHERITANCE. A REPORT ON THREE PEDIGREES = MYOPATHIE BENIGNE, AVEC TRANSMISSION AUTOSOMIQUE DOMINANTE. ETUDE DE TROIS ARBRES GENEALOGIQUESBETHLEM J; VAN WIJNGAARDEN GK.1976; BRAIN; G.B.; DA. 1976; VOL. 99; NO 1; PP. 91-100; BIBL. 9 REF.Article

ETUDE GENETIQUE D'UNE FAMILLE ATTEINTE DE MALADIE DE CHARCOT-MARIE-TOOTHGENCIK A; JAGR J; MATULOVA B et al.1974; CESKOSL. NEUROL. NEUROCHIR.; CESKOSL.; DA. 1974; VOL. 37; NO 5; PP. 316-320; ABS. RUSSE ANGL.; BIBL. 11 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