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

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

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

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

Estudios clinicos y complementarios a proposito de un caso de alcaptonuria familiar = Etude clinique et complémentaire à propos d'un cas d'alcaptonurie familiale = Clinical and complementary study of a familiar case of alcaptonuriaOROZCO, M. A; BLANZARI, R; PONSSA, G. J. R et al.Archivos argentinos de dermatologia. 1984, Vol 34, Num 1, pp 43-50, issn 0066-6750Article

Le déficit constitutionnel en protéine C: une nouvelle cause de maladie thrombo-embolique = Protein C deficiency: a new etiology for thrombotic diseasePICOT, C; SAMAMA, M.Gazette médicale de France (1969). 1983, Vol 90, Num 29, pp 2841-2844, issn 0016-5557Article

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

Chronic granulomatous disease in two sistersD'AMELIO, R; BELLAVITE, P; AIUTI, F et al.Journal of clinical immunology. 1984, Vol 4, Num 3, pp 220-227, issn 0271-9142Article

Concurrent infection in families of patients with acute toxoplasmosisSACKS, J. J.Archives of internal medicine (1960). 1984, Vol 144, Num 1, pp 35-36, issn 0003-9926Article