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4. 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]
5. Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome. Doerfler W; Wieczorek D; Gillessen-Kaesbach G; Albrecht B; Passarge E Am J Med Genet; 1997 Dec; 73(2):210-6. PubMed ID: 9409875 [TBL] [Abstract][Full Text] [Related]
6. The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome. Smeets E; Fryns JP; Van den Berghe H Genet Couns; 1996; 7(2):143-6. PubMed ID: 8831134 [TBL] [Abstract][Full Text] [Related]
7. [Floating-Harbor syndrome in a girl with somatic asymmetry]. Midro AT; Rogowska M; Hubert E; Hassman-Poznańska E; Popko J Pediatr Pol; 1995 Sep; 70(9):775-8. PubMed ID: 8657512 [TBL] [Abstract][Full Text] [Related]
8. Weaver syndrome in two Japanese children. Kondo I; Mori Y; Kuwajima K Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638 [TBL] [Abstract][Full Text] [Related]
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10. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review. Bastaki L; El-Nabi MM; Azab AS; Gouda SA; Al-Wadaani AM; Naguib KK East Mediterr Health J; 2007; 13(4):975-9. PubMed ID: 17955782 [No Abstract] [Full Text] [Related]
12. Floating-Harbor syndrome: case report. Genc G; Sarac A; Erkek Atay N; Kulali F Minerva Pediatr; 2008 Apr; 60(2):249-51. PubMed ID: 18449141 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Delineation of the da-Silva syndrome. Naritomi K; Tohma T; Goya Y; Shiroma N; Hirayama K Am J Med Genet; 1994 Feb; 49(3):313-6. PubMed ID: 8209892 [TBL] [Abstract][Full Text] [Related]
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16. [Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype]. Blanco-Barca O; Gallego-Blanco M; Ruiz-Ponte C; Barros-Angueira F; Esquete-López C; Eirís-Puñal J; Castro-Gago M Rev Neurol; 2004 Jun 1-15; 38(11):1038-42. PubMed ID: 15202082 [TBL] [Abstract][Full Text] [Related]
17. Clinical and genetic characteristics and effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome. García RJ; Kant SG; Wit JM; Mericq V J Pediatr Endocrinol Metab; 2012; 25(1-2):207-12. PubMed ID: 22570979 [TBL] [Abstract][Full Text] [Related]
18. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome? Mégarbané A; Abi Moussa M Genet Couns; 1997; 8(2):127-32. PubMed ID: 9219011 [TBL] [Abstract][Full Text] [Related]
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