Multiple Pterygium syndrome: an overviewRAMER, J. C; LADDA, R. L; DEMUTH, W. W et al.American journal of diseases of children (1960). 1988, Vol 142, Num 7, pp 794-798, issn 0002-922XArticle

Syndrome de casse-noisette = Nutcracker syndromeBERNARD, Clémence; DE SAINT ROMAN, Charlotte; GERVAISE, Alban et al.La Presse médicale (1983). 2013, Vol 42, Num 4, pp 487-488, issn 0755-4982, 2 p., CAH1Article

Síndrome de Rabson-Mendenhall = Rabson-Mendenhall syndromeAGUADO LOBO, I; GARCIA CUARTERO, B; GONZALEZ VERGAZ, A et al.Anales de pediatria (2003. Ed. impresa). 2011, Vol 74, Num 5, pp 349-350, issn 1695-4033, 2 p.Article

LAPS Syndrome and Myhre Syndrome : Two Disorders or One?LINDOR, Noralane M.American journal of medical genetics. Part A. 2009, Vol 149, Num 4, pp 798-799, issn 1552-4825, 2 p.Article

Un syndrome caveREZGUI-MARHOUL, Lamia; DOUIRA, Wiém; BOUSLAMA, Kamel et al.Concours médical (Paris). 2004, Vol 126, Num 2, pp 99-101, issn 0010-5309, 3 p.Article

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2BALLIF, Blake C; HORNOR, Sara A; GRAHAM, John M et al.Nature genetics. 2007, Vol 39, Num 9, pp 1071-1073, issn 1061-4036, 3 p.Article

Oui, il existe un syndrome de la grande exclusion = Yes, there is a syndrome of the great exclusionEMMANUELLI, Xavier.La Presse médicale (1983). 2009, Vol 38, Num 11, pp 1557-1559, issn 0755-4982, 3 p.Article

A girl with the Pitt-Rogers-Danks syndromeOORTHUYS, J. W. E; BLEEKER-WAGEMAKERS, E. M.American journal of medical genetics. 1989, Vol 32, Num 1, pp 140-141, issn 0148-7299, 2 p.Article

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndromeBAMFORTH, J. S; LEONARD, C. O; CHODIRKER, B. N et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 93-99, issn 0148-7299, 7 p.Article

Leriche SyndromeFREDERICK, Michael; NEWMAN, John; KOHLWES, Jeffrey et al.Journal of general internal medicine. 2010, Vol 25, Num 10, pp 1102-1104, issn 0884-8734, 3 p.Article

Kounis SyndromeLOPEZ, Pablo R; PEIRIS, Alan N.Southern medical journal (Birmingham, Ala. Print). 2010, Vol 103, Num 11, pp 1148-1155, issn 0038-4348, 8 p.Article

Molecular bases of progeroid syndromesNAVARRO, Claire L; CAU, Pierre; LEVYL, Nicolas et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R151-R161, NS2Article

Clinical and molecular genetic features of ARC syndromeGISSEN, Paul; TEE, Louise; FITZPATRICK, David et al.Human genetics. 2006, Vol 120, Num 3, pp 396-409, issn 0340-6717, 14 p.Article

CARD15 mutations in Blau syndromeMICELI-RICHARD, Corinne; LESAGE, Suzanne; RYBOJAD, Michel et al.Nature genetics. 2001, Vol 29, Num 1, pp 19-20, issn 1061-4036Article

Syndrome de Wellens = Wellens syndromePEYRONY, O; ELEZI, A; TABOULET, P et al.Annales françaises de médecine d'urgence. 2013, Vol 3, Num 5, issn 2108-6524, p. 321Article

DCTN1 mutations in Perry syndromeFARRER, Matthew J; HULIHAN, Mary M; TSUBOI, Yoshio et al.Nature genetics. 2009, Vol 41, Num 2, pp 163-165, issn 1061-4036, 3 p.Article

Syndrome post-poliomyélite : Handicap = Postpolio syndrome F Genêt, L. Théfenne, F Boyer : HandicapGENET, François; THEFENNE, Laurent; BOYER, François et al.La Revue du praticien (Paris). 2009, Vol 59, Num 8, pp 1085-1086, issn 0035-2640, 2 p.Article

Shapiro syndromeSAYRE SHENOY, Chetan.QJM (Oxford. 1994. Print). 2008, Vol 101, Num 1, pp 61-62, issn 1460-2725, 2 p.Article

Rumination Syndrome : An Emerging Case ScenarioATTRI, Navneet; RAVIPATI, M; AGRAWAL, Preeti et al.Southern medical journal (Birmingham). 2008, Vol 101, Num 4, pp 432-435, issn 0038-4348, 4 p.Article

Neuroleptic malignant syndromeSTRAWN, Jeffrey R; KECK, Paul E; CAROFF, Stanley N et al.The American journal of psychiatry. 2007, Vol 164, Num 6, pp 870-876, issn 0002-953X, 7 p.Article

Ganser's syndromeDWYER, Justin; REID, Steven.Lancet (British edition). 2004, Vol 364, Num 9432, pp 471-473, issn 0140-6736, 3 p.Article

Sotos syndromeTATTON-BROWN, Katrina; RAHMAN, Nazneen.European journal of human genetics. 2007, Vol 15, Num 3, pp 264-271, issn 1018-4813, 8 p.Article

Nephrogenic syndrome of inappropriate antidiuresisFELDMAN, Brian J; ROSENTHAL, Stephen M; GITELMAN, Stephen E et al.The New England journal of medicine. 2005, Vol 352, Num 18, pp 1884-1890, issn 0028-4793, 7 p.Article

Un syndrome sub-occlusif très atypique = A very atypical sub-occlusive syndromeOTT, Jean-Jacques; MAHBOUBI, Nadia; BABIN, Stéphane et al.La Revue de gériatrie. 2004, Vol 29, Num 10, pp 831-832, issn 0397-7927, 2 p.Article

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndromeARBOLEDA, Valerie A; LEE, Hane; DELL'ANGELICA, Esteban C et al.Nature genetics. 2012, Vol 44, Num 7, pp 788-792, issn 1061-4036, 5 p.Article