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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

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

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

PASSAVOY FACTOR: A HITHERTO UNRECOGNISED FACTOR NECESSARY FOR HEMOSTASIS = FACTEUR PASSAVOY: UN FACTEUR JUSQU'ICI INCONNU NECESSAIRE A L'HEMOSTASEHOUGHE C; MCPHERSON RA; ARONSON L et al.1975; LANCET; G.B.; DA. 1975; NO 7929; PP. 290-291; BIBL. 11 REF.Article

CANCER CONDORDANCE AND THE HYPOTHESIS OF AUTOSOMAL DOMINANT TRANSMISSION OF CANCER DIATHESIS IN A REMARKABLE KINDRED = CONCORDANCE DES CANCERS ET L'HYPOTHESE D'UNE TRANSMISSION DOMINANTE AUTOSOMIQUE DE LA DIATHESE CANCEREUSE DANS UNE FAMILLE REMARQUABLELYNCH HT; KAPLAN AR.1974; ONCOLOGY; SWITZ.; DA. 1974; VOL. 30; NO 3; PP. 210-216; BIBL. 7REF.Article

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

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

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

BEITRAG ZUM STUDIUM DER VERERBUNG VON BRACHYGNATHIA SUPERIOR BEI KANINCHEN = CONTRIBUTION A L'ETUDE DE LA TRANSMISSIBILITE DE LA BRACHYGNATHIE SUPERIEURE CHEZ LE LAPINGRANAT J; ZELNIK J; BULLA J et al.1974; Z. TIERZUECHT. ZUECHT.-BIOL.; DTSCH.; DA. 1974; VOL. 91; NO 1-2; PP. 131-137; ABS. ANGL.; BIBL. 7 REF.Article

MYOTONIE DYSTROPHIQUE FAMILIALENEJMARK EZ; TOKAR ZM; VASIL'EVA AF et al.1974; VRACH. DELO, U.S.S.R.; S.S.S.R.; DA. 1974; NO 7; PP. 99-103; ABS. ANGL.Article

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

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

LACK OF AN AUTOSOMAL RECESSIVE GENETIC INFLUENCE IN VERTICAL TRANSMISSION OF HEPATITIS B ANTIGEN = ABSENCE D'UNE INFLUENCE GENETIQUE AUTOSOMIQUE RECESSIVE DANS LA TRANSMISSION VERTICALE DE L'ANTIGENE DE L'HEPATITE BSTEVENS CE; BEASLEY RP.1976; NATURE; G.B.; DA. 1976; VOL. 260; NO 5553; PP. 715-716; BIBL. 18 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

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

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

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