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10. Is the frequency of Robinow syndrome relatively high in Turkey? Four more case reports. Akşit S; Aydinlioglu H; Dizdarer G; Caglayan S; Bektaşlar D; Cin A Clin Genet; 1997 Oct; 52(4):226-30. PubMed ID: 9383028 [TBL] [Abstract][Full Text] [Related]
11. Craniofacial phenotypes associated with Robinow syndrome. Conlon CJ; Abu-Ghname A; Raghuram AC; Davis MJ; Guillen DE; Sutton VR; Carvalho CMB; Maricevich RS Am J Med Genet A; 2021 Dec; 185(12):3606-3612. PubMed ID: 33237614 [TBL] [Abstract][Full Text] [Related]
18. A new syndrome. Short limbs, abnormal facial appearance, and congenital heart defect. Barrow M; Fitzsimmons JS Am J Med Genet; 1984 Jul; 18(3):431-3. PubMed ID: 6476004 [No Abstract] [Full Text] [Related]
19. Extremity anomalies associated with Robinow syndrome. Abu-Ghname A; Trost J; Davis MJ; Sutton VR; Zhang C; Guillen DE; Carvalho CMB; Maricevich RS Am J Med Genet A; 2021 Dec; 185(12):3584-3592. PubMed ID: 32974972 [TBL] [Abstract][Full Text] [Related]
20. Congenital heart disease and Robinow syndrome. Atalay S; Ege B; Imamoğlu A; Suskan E; Ocal B; Gümüş H Clin Dysmorphol; 1993 Jul; 2(3):208-10. PubMed ID: 8287182 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]