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A mild autosomal recessive form of osteopetrosisKAHLER, S. G; BURNS, J. A; AYLSWORTH, A. S et al.American journal of medical genetics. 1984, Vol 17, Num 2, pp 451-464, 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

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

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

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

Hérédité monofactorielle : construction et interprétation d'un arbre généalogique principes du conseil génétique = Monofactorial heredityEYDOUX, P.La Revue du praticien (Paris). 1991, Vol 41, Num 25, pp 2645-2653, issn 0035-2640Article

Genetic analysis of familial erythrophagocytic lymphohistiocytosisGENCIK, A; SIGNER, E; MULLER, H et al.European journal of pediatrics. 1984, Vol 142, Num 4, pp 248-252, issn 0340-6199Article

AUTOSOMAL RECESSIVE ACROCEPHALOSYNDACTYLY REVISITEDHALL JG; REED SD; SELLS CJ et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 4; PP. 423-424; BIBL. 5 REF.Article

AUTOSOMAL INHERITANCE OF PHOSPHOGLYCERATE KINASE IN THE DOMESTIC CHICKEN (GALLUS DOMESTICUS).CAM AE; COOPER DW.1978; BIOCHEM. GENET.; USA; DA. 1978; VOL. 16; NO 3-4; PP. 261-270; BIBL. 25 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

Autosomal dominant growth hormone deficiency disrupts secretory vesicles in vitro and in vivo in transgenic miceMCGUINNESS, Lindsay; MAGOULAS, Charalambos; SESAY, Abdul K et al.Endocrinology (Philadelphia). 2003, Vol 144, Num 2, pp 720-731, issn 0013-7227, 12 p.Article

Elevated n-alkanes in congenital ichthyosiform erythroderma: phenotypic differentiation of two types of autosomal recessive ichthyosisWILLIAMS, M. L; ELIAS, P. M.The Journal of clinical investigation. 1984, Vol 74, Num 1, pp 296-300, issn 0021-9738Article

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

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

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