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Journal Abstract Search
261 related items for PubMed ID: 1785626
1. Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism, and mental retardation. Imaizumi K, Kuroki Y. Am J Med Genet; 1991 Nov 01; 41(2):162-3. PubMed ID: 1785626 [No Abstract] [Full Text] [Related]
3. Another patient with an unusual syndrome of mental retardation and sparse hair? Krajewska-Walasek M, Chrzanowska K, Czermiska-Kowalska A. Clin Dysmorphol; 1996 Apr 01; 5(2):183-6. PubMed ID: 8723571 [No Abstract] [Full Text] [Related]
4. A familial syndrome of cranial, facial, oral and limb anomalies. Fitch N, Jequier S, Papageorgiou A. Clin Genet; 1976 Oct 01; 10(4):226-31. PubMed ID: 975599 [Abstract] [Full Text] [Related]
5. The radiological diagnosis of the fetal-face (= Robinow) syndrome (mesomelic dwarfism and small genitalia). Report of 3 cases. Giedion A, Battaglia GF, Bellini F, Fanconi G. Helv Paediatr Acta; 1976 Jan 01; 30(4-5):409-23. PubMed ID: 1245439 [Abstract] [Full Text] [Related]
6. Costello syndrome and facio-cutaneous-skeletal syndrome. Philip N, Mancini J. Am J Med Genet; 1993 Aug 15; 47(2):174-5. PubMed ID: 8213902 [No Abstract] [Full Text] [Related]
7. [Bird headed dwarfism in Seckel syndrome. Nosologic difficulties]. Parent P, Moulin S, Munck MR, de Parscau L, Alix D. Arch Pediatr; 1996 Jan 15; 3(1):55-62. PubMed ID: 8745829 [Abstract] [Full Text] [Related]
8. Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome? van Maldergem L, Wetzburger C, Verloes A, Fourneau C, Gillerot Y. Clin Genet; 1992 Jan 15; 41(1):22-4. PubMed ID: 1633641 [Abstract] [Full Text] [Related]
9. A Japanese patient with the Costello syndrome. Okamoto N, Chiyo H, Imai K, Otani K, Futagi Y. Hum Genet; 1994 May 15; 93(5):605-6. PubMed ID: 8168845 [Abstract] [Full Text] [Related]
10. [Associated malformations of the head and extremities]. Tridon P. J Genet Hum; 1974 Dec 15; 22(4):365-80. PubMed ID: 4282383 [No Abstract] [Full Text] [Related]
12. The congenital triangular deformity of the tubular bones of hand and foot. Jaeger M, Refior HJ. Clin Orthop Relat Res; 1971 Dec 15; 81():139-50. PubMed ID: 4332222 [No Abstract] [Full Text] [Related]
13. Specific acromesomelia with facial and renal anomalies: a new syndrome. Pfeiffer RA, Hirschfelder H, Rott HD. Clin Dysmorphol; 1995 Jan 15; 4(1):38-43. PubMed ID: 7735504 [Abstract] [Full Text] [Related]
15. RAPADILINO syndrome. Vargas FR, de Almeida JC, Llerena Júnior JC, Reis DF. Am J Med Genet; 1992 Dec 01; 44(6):716-9. PubMed ID: 1481838 [Abstract] [Full Text] [Related]
16. Dwarfism, rhizomelic limb shortness, and abnormal face: new short stature syndrome sharing some manifestations with Robinow syndrome. Turnpenny PD, Thwaites RJ. Am J Med Genet; 1992 Mar 01; 42(5):724-7. PubMed ID: 1632447 [Abstract] [Full Text] [Related]
17. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome]. Franceschini P, Franceschini D. Minerva Pediatr; 1994 Dec 01; 46(12):579-80. PubMed ID: 7731422 [No Abstract] [Full Text] [Related]
18. [Rubinstein-Taybi syndrome (a propos of 4 cases)]. Levy-Leblond E, D'Oelsnitz M, Vaillant JM, Maroteaux P. Arch Fr Pediatr; 1969 May 01; 26(5):523-35. PubMed ID: 5363526 [No Abstract] [Full Text] [Related]