These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
191 related articles for article (PubMed ID: 16650233)
21. CFC index for the diagnosis of cardiofaciocutaneous syndrome. Kavamura MI; Peres CA; Alchorne MM; Brunoni D Am J Med Genet; 2002 Sep; 112(1):12-6. PubMed ID: 12239713 [TBL] [Abstract][Full Text] [Related]
22. Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes. Marchegiani S; Davis T; Tessadori F; van Haaften G; Brancati F; Hoischen A; Huang H; Valkanas E; Pusey B; Schanze D; Venselaar H; Vulto-van Silfhout AT; Wolfe LA; Tifft CJ; Zerfas PM; Zambruno G; Kariminejad A; Sabbagh-Kermani F; Lee J; Tsokos MG; Lee CC; Ferraz V; da Silva EM; Stevens CA; Roche N; Bartsch O; Farndon P; Bermejo-Sanchez E; Brooks BP; Maduro V; Dallapiccola B; Ramos FJ; Chung HY; Le Caignec C; Martins F; Jacyk WK; Mazzanti L; Brunner HG; Bakkers J; Lin S; Malicdan MC; Boerkoel CF; Gahl WA; de Vries BB; van Haelst MM; Zenker M; Markello TC Am J Hum Genet; 2015 Jul; 97(1):99-110. PubMed ID: 26119818 [TBL] [Abstract][Full Text] [Related]
23. Cryptophthalmos syndrome. Wiznitzer A; Mazor M; Carmi R; Leiberman JR Isr J Med Sci; 1985 Jul; 21(7):636-7. PubMed ID: 4044227 [No Abstract] [Full Text] [Related]
27. [Ciliary hypertrichosis and facial dysmorphia associated with diffuse, congenital hypertrichosis: Ambras syndrome?]. Boui M; Ghfir M; Sedrati O Ann Dermatol Venereol; 2009 May; 136(5):481-2. PubMed ID: 19442813 [No Abstract] [Full Text] [Related]
28. [Costello syndrome. Presentation of a case with a follow-up of 35 years]. Pascual-Castroviejo I; Pascual-Pascual S Neurologia; 2005 Apr; 20(3):144-8. PubMed ID: 15815950 [TBL] [Abstract][Full Text] [Related]
29. Ablepharon-macrostomia syndrome. Stevens CA; Sargent LA Am J Med Genet; 2002 Jan; 107(1):30-7. PubMed ID: 11807864 [TBL] [Abstract][Full Text] [Related]
30. Lateral facial clefts: a case report. de Die-Smulders CE; Moog U; Engelen JJ; Peters JJ; Damen A; Vos W; Fryns JP Genet Couns; 2001; 12(2):163-5. PubMed ID: 11491312 [TBL] [Abstract][Full Text] [Related]
31. A case of Barber-Say syndrome in a male Japanese newborn. Suga K; Shono M; Goji A; Matsuura S; Inoue M; Kawahito M; Kinoshita M; Takeda M; Mori K Clin Case Rep; 2014 Oct; 2(5):224-7. PubMed ID: 25614816 [TBL] [Abstract][Full Text] [Related]
32. [Ambras syndrome--a form of generalised congenital hypertrichosis]. Torbus O; Sliwa F Pol Merkur Lekarski; 2002 Mar; 12(69):238-40. PubMed ID: 12053598 [TBL] [Abstract][Full Text] [Related]
33. [Kabuki syndrome in the differential diagnosis of neonatal hypotonia]. Aguilera Albesa S; Botella Astorqui MP; Ocio Ocio I An Pediatr (Barc); 2009 Jan; 70(1):91-3. PubMed ID: 19174128 [No Abstract] [Full Text] [Related]
34. Differentiation of congenital hypertrichosis from Ambras syndrome. Baumeister FA; Stengel-Rutkowski S Clin Genet; 1994 Dec; 46(6):441. PubMed ID: 7889664 [No Abstract] [Full Text] [Related]
35. A whistling face syndrome case with bilateral skin dimples. Buyukavci M; Tan H; Eren S; Balci S Genet Couns; 2005; 16(1):71-3. PubMed ID: 15844782 [TBL] [Abstract][Full Text] [Related]
36. [Potter's syndrome. Description of a clinical case]. Di Battista C; Guastaferro N; Marcelli P; Di Saverio P Minerva Pediatr; 1981 Jun; 33(12):583-6. PubMed ID: 7266438 [No Abstract] [Full Text] [Related]
37. Another case of the human homologue of the mouse mutant disorganization. Teebi AS; Elliott AM Am J Med Genet; 1996 Jan; 61(1):94. PubMed ID: 8741929 [No Abstract] [Full Text] [Related]