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Results 1 to 25 of 34879

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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 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

Signaling via Shc family adapter proteinsRAVICHANDRAN, Kodi S.Oncogene (Basingstoke). 2001, Vol 20, Num 44, pp 6322-6330, issn 0950-9232Article

Ectrodactyly in sisters and half sistersMUFTI, M. H; WOOD, S. K.Journal of medical genetics. 1987, Vol 24, Num 4, pp 220-224, issn 0022-2593Article

The distribution of nutrient intake within familiesNELSON, M.British journal of nutrition. 1986, Vol 55, Num 2, pp 267-277, issn 0007-1145Article

La dysostose cléido-crânienne. Contribution à son étude à propos de deux cas personnels (une forme isolée et une forme familiale) = Cleido-cranial dysostosis. Two case reports (one isolated and one familial form)TEYTON, L; MORA, J.-J; LOYAU, G et al.La Revue de médecine interne (Paris). 1984, Vol 5, Num 1, pp 76-82, issn 0248-8663Article

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

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

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

An exceptional mutational event leading to Chanarin―Dorfman syndrome in a large consanguineous familySAMUELOV, L; FUCHS-TELEM, D; SARIG, O et al.British journal of dermatology (1951). 2011, Vol 164, Num 6, pp 1390-1392, issn 0007-0963, 3 p.Article

Expression of trefoil factor family 1, 2, and 3 peptide is augmented in hepatolithiasisSASAKI, Motoko; IKEDA, Hiroko; OHIRA, Shusaku et al.Peptides (New York, NY. 1980). 2004, Vol 25, Num 5, pp 763-770, issn 0196-9781, 8 p.Article

A unified framework for transmission-disequilibrium test analysis of discrete and continuous traitsYING LIU; TRITCHLER, David; BULL, Shelley B et al.Genetic epidemiology. 2002, Vol 22, Num 1, pp 26-40, issn 0741-0395Article

Recurrence of different mosaic structural chromosomal anomalies within a familySMITH, A; COHEN, M; DEN DULK, G et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 36-38, issn 0003-3995, 3 p.Article

Osteogenesis imperfecta with unusual skeletal lesions: report of three familiesLEVIN, L. S; WRIGHT, J. M; BYRD, D. L et al.American journal of medical genetics. 1985, Vol 21, Num 2, pp 257-269, issn 0148-7299Article

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