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Results 1 to 25 of 42557

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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

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

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

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

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

Cohort Profile: The Hawai'i Family Study of CognitionONOYE, Jane Mm; HISHINUMA, Earl S; MCARDLE, John J et al.International journal of epidemiology. 2014, Vol 43, Num 6, pp 1726-1735, issn 0300-5771, 10 p.Article

Type C brachydactyly transmitted through four generationsSANZ, J; GILGENKRANTZ, S.Annales de génétique (Paris). 1988, Vol 31, Num 1, pp 43-46, issn 0003-3995Article

A new case of the osteodysplastic imordial dwarfism type IIWILLEMS, P. J; ROUWE, C; SMIT, G. P. A et al.American journal of medical genetics. 1987, Vol 26, Num 4, pp 819-824, issn 0148-7299Article

Familial dilated cardiomyopathyVOSS, E. G; REDDY, C. V. R; DETRANO, R et al.The American journal of cardiology. 1984, Vol 54, Num 3, pp 456-457, issn 0002-9149Article

Chronic arsenic poisoning from tube-well waterGARAT, R; CHAKRABORTY, A. K; DEY, S. B et al.Journal of the Indian Medical Association. 1984, Vol 82, Num 1, pp 34-35, issn 0019-5847Article

Primary and familial hypoalphalipoproteinemiaTHIRD, J. L. H. C; MONTAG, J; FLYNN, M et al.Metabolism, clinical and experimental. 1984, Vol 33, Num 2, pp 136-146, issn 0026-0495Article

Dysplasie dyssegmentaire: à propos de 2 cas familiaux dévolution létale = Dyssegmental dwarfism. Two lethal cases in the same sibshipBUENO, M; ARGEMI, J; MAROTEAUX, P et al.Archives françaises de pédiatrie. 1984, Vol 41, Num 4, pp 269-271, issn 0003-9764Article

Les polyposes recto-coliques familiales = Family polyposes of the colon and rectumDJEMLN; MESTIRI, S; GARGOURI, M et al.Tunisie médicale. 1984, Vol 62, Num 4, pp 289-295, issn 0041-4131Article

Conjugal progressive systemic sclerosis (Scleroderma): report of the disease in husband and wifeCHRISTY, W. C; RODNAN, G. P.Arthritis and rheumatism. 1984, Vol 27, Num 10, pp 1180-1182, issn 0004-3591Article

Gene extinction and allelic origins in complex genealogiesTHOMPSON, E. A.Proceedings of the Royal society of London. Series B. Biological sciences. 1983, Vol 219, Num 1216, pp 241-251, issn 0080-4649Article

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