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

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

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

Family study of subthreshold psychopathology in a community sampleSHANKMAN, S. A; KLEIN, D. N; LEWINSOHN, P. M et al.Psychological medicine (Print). 2008, Vol 38, Num 2, pp 187-198, issn 0033-2917, 12 p.Article

The IL-17 cytokine familyGAFFEN, Sarah L; KRAMER, Jill M; YU, Jeffrey J et al.Vitamins and hormones. 2006, Vol 74, pp 255-282, issn 0083-6729, 28 p.Article

Editorial comment: unstable premutation in achondroplasia: penetrance vs phenotranceOPITZ, J. M.American journal of medical genetics. 1984, Vol 19, Num 2, pp 251-254, issn 0148-7299Article

Wayward Effect of Polymorphism (TA)₈ in the Promoter Region of UGT1A1 Gene in a Mexican FamilyTINTOS-HERNANDEZ, J. A; PEREA, F. J; IBARRA, B et al.West indian medical journal. 2012, Vol 61, Num 1, pp 81-83, issn 0043-3144, 3 p.Article

Rarely Shared between Family MembersGOTTSCHLING, Marc; GÖKER, Markus; KÖHLER, Anja et al.Journal of investigative dermatology. 2009, Vol 129, Num 10, pp 2427-2434, issn 0022-202X, 8 p.Article

Familial pemphigus vulgarisBRENNER, S; DORFMAN, B; HIMELFARB, M et al.Dermatologica. 1985, Vol 171, Num 1, pp 38-40, issn 0011-9075Article

Hypersecretion of gastric acid in a representative Finnish family sampleKEKKI, M; SIPPONEN, P; SIURALA, M et al.Scandinavian journal of gastroenterology. 1985, Vol 20, Num 4, pp 478-484, issn 0036-5521Article

Adrenoleukodystrophie und Adrenomyeloneuropathie bei zwei Brüdern = Adrénoleucodystrophie et adrénomyéloneuropathie chez deux frères = Adrenoleukodystrophy and adrenomyeloneuropathy in two siblingsLEIPNER, N; KÖSTER, O; ROSSKAMP, R et al.RöFo. Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin. 1984, Vol 140, Num 3, pp 341-342, issn 0340-1618Article

Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generationsMANGANO, L; PALMERI, S; DOTTI, M. T et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 67-71, issn 0148-7299, 5 p.Article

Cervical auricles in a familyOISO, Naoki; KAWADA, Akira.EJD. European journal of dermatology. 2012, Vol 22, Num 3, pp 395-396, issn 1167-1122, 2 p.Article