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Zur Frage der Erblichkeit der Vitiligo = Le problème de l'hérédité du vitiligo = The question of heredity in vitiligoSALAMON, T; HADZISELIMOVIC, R; HALEPOVIC, E et al.Hautarzt. 1989, Vol 40, Num 3, pp 141-145, issn 0017-8470Article

A role for MLH3 in hereditary nonpolyposis colorectal cancerYING WU; BERENDS, Maran J. W; BUYS, Charles H. C. M et al.Nature genetics. 2001, Vol 29, Num 2, pp 137-138, issn 1061-4036Article

Hereditary hormone excess : Genes, molecular pathways, and syndromesMARX, Stephen J; SIMONDS, William F.Endocrine reviews. 2005, Vol 26, Num 5, pp 615-661, issn 0163-769X, 47 p.Article

Gastroduodenal polyps in familial polyposis coliGAHTAN, V; NOCHOMOVITZ, L. E; ROBINSON, A. M et al.The American surgeon. 1989, Vol 55, Num 5, pp 278-280, issn 0003-1348, 3 p.Article

TOM : enhancement and extension of a tool suite for in silico approaches to multigenic hereditary disordersMASOTTI, Daniele; NARDINI, Christine; ROSSI, Simona et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 3, pp 428-429, issn 1367-4803, 2 p.Article

Les cancers héréditaires vus par le pathologisteBIBEAU, Frédéric.Annales de pathologie (Print). 2010, Vol 30, Num NOV, issn 0242-6498, S75-S76, HSConference Paper

Inherited traits affecting platelet functionSALLES, Isabelle I; FEYS, Hendrik B; ISERBYT, Brecht F et al.Blood reviews. 2008, Vol 22, Num 3, pp 155-172, issn 0268-960X, 18 p.Article

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)VITHANA, Eranga N; MORGAN, Patricio; SALTO-TELLEZ, Manuel et al.Nature genetics. 2006, Vol 38, Num 7, pp 755-757, issn 1061-4036, 3 p.Article

Hereditary auto-inflammatory disorders and biologicsCHURCH, Leigh D; CHURCHMAN, Sarah M; HAWKINS, Philip N et al.Springer seminars in immunopathology. 2006, Vol 27, Num 4, pp 494-508, issn 0344-4325, 15 p.Article

Inherited thrombocytopenia : Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radiiGEDDIS, Amy E.Seminars in hematology. 2006, Vol 43, Num 3, pp 196-203, issn 0037-1963, 8 p.Article

Naissance de la médecine prédictive ou le rêve prédictifKLARSFELD, A.Prévenir (Marseille). 1993, Num 24, pp 45-47, issn 0247-2406Article

A new congenital dyserythropoietic anaemiaOHISALO, J. J; VIITALA, J; LINTULA, R et al.British journal of haematology. 1988, Vol 68, Num 1, pp 111-114, issn 0007-1048Article

Etude clinicogénétique du cancer du côlon. III. Tumeurs malignes primitives multiples et héréditéBELEV, N. F; GAR'KAVTSEVA, R. F; SAMOTYYA, E. E et al.Genetika. 1986, Vol 22, Num 12, pp 2847-2851, issn 0016-6758Article

Hereditary angioedema: polymorphismEGIDIO FABIANI, J; OSCAR SIMKIN, G; LEONI, J et al.Annals of allergy. 1985, Vol 55, Num 6, pp 830-834, issn 0003-4738Article

The Human Phenotype Ontology : A Tool for Annotating and Analyzing Human Hereditary DiseaseROBINSON, Peter N; KÖHLER, Sebastian; BAUER, Sebastian et al.American journal of human genetics. 2008, Vol 83, Num 5, pp 610-615, issn 0002-9297, 6 p.Article

RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumorsDE GROOT, Jan Willem B; LINKS, Thera P; PLUKKER, John T. M et al.Endocrine reviews. 2006, Vol 27, Num 5, pp 535-560, issn 0163-769X, 26 p.Article

Naissance de la médecine prédictive ou le rêve prédictifKLARSFELD, A.Prévenir (Marseille). 1993, Num 24, pp 45-47, issn 0247-2406Article

Conditional graph connectivity relative to hereditary propertiesOELLERMANN, O. R.Networks (New York, NY). 1991, Vol 21, Num 2, pp 245-255, issn 0028-3045Article

Die verschiedenen Allel- und Genbeziehungen in ihrer Auswirkung auf die MerkmalsausprägungSKIEBE, K.Biologisches Zentralblatt. 1990, Vol 109, Num 5, pp 399-405, issn 0006-3304Article

Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathyWILSON, G. N; DE CHADAREVIAN, J.-P; KAPLAN, P et al.American journal of medical genetics. 1989, Vol 32, Num 3, pp 395-401, issn 0148-7299, 7 p.Article

Antithrombin III Alger: a new case of Arg 47→Cys mutationBRUNEL, F; DUCHANGE, N; FISCHER, A.-M et al.American journal of hematology. 1987, Vol 25, Num 2, pp 223-224, issn 0361-8609Article

Chromosome studies in inherited nonpolyposis colon cancer syndromeLUKEIS, R; GARSON, O. M; MACRAE, F. A et al.Cancer genetics and cytogenetics. 1987, Vol 27, Num 1, pp 111-124, issn 0165-4608Article

Familial hairy cell leukemiaBEGLEY, C. G; TAIT, B; CRAPPER, R. M et al.Leukemia research. 1987, Vol 11, Num 11, pp 1027-1029, issn 0145-2126Article

Two hereditary spinal diseases producing kyphosis during adolescenceNIELSEN, O. G; PILGAARD, P.Acta paediatrica scandinavica. 1987, Vol 76, Num 1, pp 133-136, issn 0001-656XArticle

Les cancers héréditaires de la sphère gynécologique vus par le pathologisteSABOURIN, Jean-Christophe.Annales de pathologie (Print). 2010, Vol 30, Num NOV, issn 0242-6498, S88-S89, HSConference Paper

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