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

A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosisCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1989, Vol 26, Num 5, pp 339-342, issn 0022-2593, 4 p.Article

GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible new recessively inherited MCA/MR syndromeVERLOES, A; DELFORTRIE, J; LAMBOTTE, C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 15-18, issn 0148-7299, 4 p.Article

A combinatorial method for grouping cases with multiple malformationsWINTER, R. M; CLARK, R. D; ASHLEY, K et al.Journal of medical genetics. 1988, Vol 25, Num 2, pp 118-121, issn 0022-2593Article

Syndromology: an updated conceptual overview. III: Syndrome delineationCOHEN, M. M. JR.International journal of oral and maxillofacial surgery. 1989, Vol 18, Num 5, pp 281-285, issn 0901-5027Article

Nanisme microcéphalique, arriération sévère, hypertonie, obésité et hypog&nitalisme chez deux frères : un nouveau syndrome? = Two brothers with severe mental and growth retardation, microcephaly, hypertonicity, obesity and hypogenitalism: a new syndromeDELOZIER-BLANCHET, C. D; HAENGGELI, C. A; ENGEL, E et al.Journal de génétique humaine. 1989, Vol 37, Num 4-5, pp 353-365, issn 0021-7743, 13 p.Article

Myelodyspastic syndrome with complex cytogeneticsLAZO-LANGNER, Alejandro.Blood. 2012, Vol 120, Num 23, issn 0006-4971, p. 4458Article

Niikawa-Kuroki (Kabuki make-up) syndromeMULVIHILL, J. J; KAISER-KUPFER, M. I.American journal of medical genetics. 1989, Vol 33, Num 3, issn 0148-7299, 425Article

Cardiac involvement in Coffin-Lowry syndromeKRAJEWSKA-WALASEK, M; KUBICKA, K; RYZKO, J et al.European journal of pediatrics. 1988, Vol 147, Num 4, issn 0340-6199, 448Article

Síndrome de Werner = Le syndrome de Werner = The Werner syndromeMARQUES, L; MESQUITA-GUIMARAES, J; FERREIRA, M. R et al.Medicina cutánea ibero-latino-americana. 1987, Vol 15, Num 3, pp 208-212, issn 0210-5187Article

Cowden syndrome: clinical and pathological considerations in two new casesBAGAN, J. V; PENARROCHA, M; VERA-SEMPERE, F et al.Journal of oral and maxillofacial surgery. 1989, Vol 47, Num 3, pp 291-294, issn 0278-2391Article

Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patientsNIIKAWA, N; KUROKI, Y; IWAMA, Y et al.American journal of medical genetics. 1988, Vol 31, Num 3, pp 565-589, issn 0148-7299Article

New syndromes from old: evaluation of heterogeneity and variability in syndrome definition and delineationTORIELLO, H. V.American journal of medical genetics. Supplement. 1988, Num 4, pp 55-70, issn 1040-3787Article

Additional EFNB1 Mutations in Craniofrontonasal SyndromeWALLIS, Deeann; LACBAWAN, Felicitas; CAREY, John C et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 2008-2012, issn 1552-4825, 5 p.Article

Respiratory aspects of Shwachman's syndrome in adultsWIGGINS, J; GEDDES, D. M.The European respiratory journal. 1989, Vol 2, Num 3, pp 285-288, issn 0903-1936Article

Keutel syndrome: a report of four casesKHOSROSHAHI, H. E; ULUOGLU, O; OLGUNTURK, R et al.European journal of pediatrics. 1989, Vol 149, Num 3, pp 188-191, issn 0340-6199, 4 p.Article

Impact of complex genetic conditions on public healthVOGEL, F.Clinical genetics. 1989, Vol 36, Num 5, pp 392-404, issn 0009-9163, 13 p.Conference Paper

Bleeding diathesis in Noonan syndrome: a common associationWITT, D. R; MCGILLIVRAY, B. C; ALLANSON, J. E et al.American journal of medical genetics. 1988, Vol 31, Num 2, pp 305-317, issn 0148-7299Article

Syndromology: an updated conceptual overview. X : ReferencesCOHEN, M. M. JR.International journal of oral and maxillofacial surgery. 1990, Vol 19, Num 2, pp 89-96, issn 0901-5027Article

Epigenetics as a unifying principle in the aetiology of complex traits and diseases : PlasticityPETRONIS, Arturas.Nature (London). 2010, Vol 465, Num 7299, pp 721-727, issn 0028-0836, 7 p.Article

Genetics of the polymicrogyria syndromesJANSEN, A; ANDERMANN, E.Journal of medical genetics. 2005, Vol 42, Num 5, pp 369-378, issn 0022-2593, 10 p.Article

European meeting on dysmorphologyGenetic counseling. 1994, Vol 5, Num 1, pp 97-122, issn 1015-8146Conference Proceedings

New syndromes. II: European syndromesBEEMER, F. A.American journal of medical genetics. Supplement. 1988, Num 4, pp 71-84, issn 1040-3787Article

Holzgreve-Wagner-Rehder syndrome: potter sequence associated with persistent buccopharyngeal membrane. A second observationLEGIUS, E; MOERMAN, P; FRYNS, J. P et al.American journal of medical genetics. 1988, Vol 31, Num 2, pp 269-272, issn 0148-7299, 4 p.Article