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Results 1 to 25 of 44247

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Reticulate acropigmentation of Kitamura: a report of two familiesBAJAJ, A. K; GUPTA, S. C.Dermatologica. 1984, Vol 168, Num 5, pp 247-249, issn 0011-9075Article

Familial streblodactylyDONOFRIO, P; AYALA, F.Acta dermato-venereologica. 1983, Vol 63, Num 4, pp 361-363, issn 0001-5555Article

Inherited isolated hyperphosphatasemiaKRUSE, K.Acta paediatrica scandinavica. 1983, Vol 72, Num 6, pp 833-835, issn 0001-656XArticle

A second family with hemoglobin WillametteMARTINEZ, G; CANIZARES, M. E; COLOMBO, B et al.Hemoglobin. 1984, Vol 8, Num 2, pp 193-195, issn 0363-0269Article

Hemoglobin Kansas in a japanese familyISHIGURO, K; OHBA, Y; HATTORI, Y et al.Hemoglobin. 1983, Vol 7, Num 6, pp 573-579, issn 0363-0269Article

Recovery and persistence of stuttering among relatives of stutterersSEIDER, R. A; GLADSTIEN, K. L; KIDD, K. K et al.The Journal of speech and hearing disorders. 1983, Vol 48, Num 4, pp 402-409, issn 0022-4677Article

Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasiasFRYNS, J. P; HOFKENS, G; FABRY, G et al.Clinical genetics. 1988, Vol 33, Num 1, pp 57-59, issn 0009-9163Article

A new acro-cranio-facial dysostosis syndrome insistersKAPLAN, P; PLAUCHU, H; FITCH, N et al.American journal of medical genetics. 1988, Vol 29, Num 1, pp 95-106, issn 0148-7299Article

L'ostéomésopycnose (ostéosclérose axiale constitutionnelle) 2 nouvelles observations familiales = Ostéomesopyknosis (inherited axial osteosclerosis). A report of two new familial casesDELCAMBRE, B; FLIPO, R. M; LEROUX, J. L et al.Rhumatologie (Aix-les-Bains). 1987, Vol 39, Num 9, pp 261-265, issn 0249-7581Article

Emery-Dreifuss muscular dystrophy: report of five cases in a family and review of the literatureMERLINI, L; GRANATA, C; DOMINICI, P et al.Muscle & nerve. 1986, Vol 9, Num 6, pp 481-485, issn 0148-639XArticle

Metachondromatosis: report of four casesBASSETT, G. S; COWELL, H. R.Journal of bone and joint surgery. American volume. 1985, Vol 67, Num 5, pp 811-814, issn 0021-9355Article

Un nouveau déficit familial en prékallicréine (F. Fletcher) = Familial deficiency Fletcher factor deficiencyALEXANDRE, P; RAFFOUX, C; BRIQUEL, M. E et al.Annales médicales de Nancy et de l'Est. 1983, Vol 22, pp 421-424, issn 0221-3796Article

A family with diffuse partial woolly hairORMEROD, A. D; MAIN, R. A; RYDER, M. L et al.British journal of dermatology (1951). 1987, Vol 116, Num 3, pp 401-405, issn 0007-0963Article

Skin peeling syndrome in a Kurdish familyHACHAM-ZADEH, S; HOLUBAR, K.Archives of dermatology (1960). 1985, Vol 121, Num 4, pp 545-546, issn 0003-987XArticle

Une observation d'acrocéphalosyndactylie familiale = Report of a case of familial acrocephalosyndactylyLE MERRER, M; MAROTEAUX, P; FREZAL, J et al.Annales de pédiatrie (Paris). 1983, Vol 30, Num 9, pp 695-697, issn 0066-2097Article


How to choose a job after a GI fellowship (weighing family and city life against salary and research)SONNENBERG, Amnon.Gastrointestinal endoscopy (Print). 2009, Vol 69, Num 3, pp 526-529, issn 0016-5107, 4 p., 1Article

The new plant virus family Flexiviridae and assessment of molecular criteria for species demarcationADAMS, M. J; ANTONIW, J. F; BAR-JOSEPH, M et al.Archives of virology. 2004, Vol 149, Num 5, pp 1045-1060, issn 0304-8608, 16 p.Article

Familial expansile osteolysis: a new dysplasiaOSTERBERG, P. H; WALLACE, R. G. H; ADAMS, D. A et al.Journal of bone and joint surgery. British volume. 1988, Vol 70, Num 2, pp 255-260, issn 0301-620XArticle

Epidemiologic study of the mallet finger deformityJONES, N. F; PETERSON, J.The Journal of hand surgery (St. Louis, Mo.). 1988, Vol 13, Num 3, pp 334-338, issn 0363-5023Article

A family study of hidradenitis suppurativaFITZSIMMONS, J. S; GUILBERT, P. R.Journal of medical genetics. 1985, Vol 22, Num 5, pp 367-373, issn 0022-2593Article

Osteoporosis-pseudoglioma syndrome: report of three affected sibs and an overviewFRONTALI, M; STOMEO, C; DALLAPICCOLA, B et al.American journal of medical genetics. 1985, Vol 22, Num 1, pp 35-47, issn 0148-7299Article

Familial malignant atrophic papulosisNEWTON, J. A; BLACK, M. M.Clinical and experimental dermatology (Print). 1984, Vol 9, Num 3, pp 298-299, issn 0307-6938Article

Low natural cytotoxicity of peripheral blood mononuclear cells in individuals with high familial incidences of cancer = Cytotoxicité naturelle faible des cellules mononucléaires sanguines chez les individus ayant une proportion élevée de cancers dans la familleSTRAYER, D. R; CARTER, W. A; MAYBERRY, S. D et al.Cancer research (Baltimore). 1984, Vol 44, Num 1, pp 370-374, issn 0008-5472Article

Neural tube defects as an X-linked conditionBARAITSER, M; BURN, J.American journal of medical genetics. 1984, Vol 17, Num 1, pp 383-385, issn 0148-7299Article

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