89 related articles for article (PubMed ID: 9017917)
1. The Williams syndrome: an Italian collaborative study.
Franceschini P; Guala A; Vardeu MP; Signorile F; Franceschini D; Mastroiacovo P; Gianotti A; Livini E; Lalatta F; Selicorni A; Andria G; Scarano G; Della Monica M; Rizzo R; Zelante L; Stabile M; Gabrielli O; Neri G
Minerva Pediatr; 1996 Oct; 48(10):421-8. PubMed ID: 9017917
[TBL] [Abstract][Full Text] [Related]
2. Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.
Ferrero GB; Biamino E; Sorasio L; Banaudi E; Peruzzi L; Forzano S; di Cantogno LV; Silengo MC
Eur J Med Genet; 2007; 50(5):327-37. PubMed ID: 17625998
[TBL] [Abstract][Full Text] [Related]
3. [Williams syndrome without cardiovascular abnormalities].
Cincinnati P; Genuardi M; Rutiloni C
Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296
[TBL] [Abstract][Full Text] [Related]
4. Clinical and behavioral characteristics in FG syndrome.
Graham JM; Superneau D; Rogers RC; Corning K; Schwartz CE; Dykens EM
Am J Med Genet; 1999 Aug; 85(5):470-5. PubMed ID: 10405444
[TBL] [Abstract][Full Text] [Related]
5. Niikawa-Kuroki syndrome.
Roccella M
Minerva Pediatr; 1999; 51(7-8):271-8. PubMed ID: 10634060
[TBL] [Abstract][Full Text] [Related]
6. [Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects].
van Hagen JM; Govaerts LC; de Coo IF; Gille JJ; Nieuwint AW; Madan K
Ned Tijdschr Geneeskd; 2001 Mar; 145(9):396-400. PubMed ID: 11253493
[TBL] [Abstract][Full Text] [Related]
7. [Williams-Beuren syndrome: a multidisciplinary approach].
Lacroix A; Pezet M; Capel A; Bonnet D; Hennequin M; Jacob MP; Bricca G; Couet D; Faury G; Bernicot J; Gilbert-Dussardier B
Arch Pediatr; 2009 Mar; 16(3):273-82. PubMed ID: 19097873
[TBL] [Abstract][Full Text] [Related]
8. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
Milà M; Carrió A; Sánchez A; Gómez D; Jiménez D; Estivill X; Ballesta F
Med Clin (Barc); 1999 Jun; 113(2):46-9. PubMed ID: 10425618
[TBL] [Abstract][Full Text] [Related]
9. [Genetic diagnosis of Williams syndrome].
Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G
Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487
[TBL] [Abstract][Full Text] [Related]
10. Williams syndrome and the elastin gene in Thai patients.
Ruangdaraganon N; Tocharoentanaphol C; Kotchabhakdi N; Khowsathit P
J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S174-8. PubMed ID: 10730539
[TBL] [Abstract][Full Text] [Related]
11. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Van der Aa N; Rooms L; Vandeweyer G; van den Ende J; Reyniers E; Fichera M; Romano C; Delle Chiaie B; Mortier G; Menten B; Destrée A; Maystadt I; Männik K; Kurg A; Reimand T; McMullan D; Oley C; Brueton L; Bongers EM; van Bon BW; Pfund R; Jacquemont S; Ferrarini A; Martinet D; Schrander-Stumpel C; Stegmann AP; Frints SG; de Vries BB; Ceulemans B; Kooy RF
Eur J Med Genet; 2009; 52(2-3):94-100. PubMed ID: 19249392
[TBL] [Abstract][Full Text] [Related]
12. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
13. [William's syndrome. Report of a case with family involvement].
Onís Vilches MC; Rubio Cuadrado MV; Martínez de la Iglesia J; López Granados A
Rev Clin Esp; 1998 Feb; 198(2):91-4. PubMed ID: 9558923
[TBL] [Abstract][Full Text] [Related]
14. MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions.
Kirchhoff M; Bisgaard AM; Bryndorf T; Gerdes T
Eur J Med Genet; 2007; 50(1):33-42. PubMed ID: 17090394
[TBL] [Abstract][Full Text] [Related]
15. Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome.
Mori PG; Priolo M; Lerone M; Pasino M; Caroli F; Cusano R; Seri M; Silengo MC
Am J Med Genet; 1999 Nov; 87(1):36-9. PubMed ID: 10528244
[TBL] [Abstract][Full Text] [Related]
16. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
[TBL] [Abstract][Full Text] [Related]
17. Outcome in adult life for people with Williams syndrome-- results from a survey of 239 families.
Howlin P; Udwin O
J Intellect Disabil Res; 2006 Feb; 50(Pt 2):151-60. PubMed ID: 16403203
[TBL] [Abstract][Full Text] [Related]
18. [Hypomelanosis of Ito. A possibly under-diagnosed heterogeneous neurocutaneous syndrome].
Gómez-Lado C; Eirís-Puñal J; Blanco-Barca O; del Río-Latorre E; Fernández-Redondo V; Castro-Gago M
Rev Neurol; 2004 Feb 1-15; 38(3):223-8. PubMed ID: 14963848
[TBL] [Abstract][Full Text] [Related]
19. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP
Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297
[TBL] [Abstract][Full Text] [Related]
20. Neurocranial morphology and growth in Williams syndrome.
Axelsson S; Kjaer I; Heiberg A; Bjørnland T; Storhaug K
Eur J Orthod; 2005 Feb; 27(1):32-47. PubMed ID: 15743861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
