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2. Limb pterygium syndromes: a review and report of eleven patients. Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793 [TBL] [Abstract][Full Text] [Related]
3. [The multiple pterygium syndrome or Escobar syndrome: a case report]. Capilupi B; Olappi G; Cornaglia A; Novati GP Pediatr Med Chir; 1998; 20(4):295-8. PubMed ID: 9866856 [TBL] [Abstract][Full Text] [Related]
4. Two sisters with Escobar syndrome. Spranger S; Spranger M; Meinck HM; Tariverdian G Am J Med Genet; 1995 Jul; 57(3):425-8. PubMed ID: 7677145 [TBL] [Abstract][Full Text] [Related]
6. Multiple pterygium syndrome. Chen H; Chang CH; Misra RP; Peters HA; Grijalva NS; Opitz JM Am J Med Genet; 1980; 7(2):91-102. PubMed ID: 7468651 [TBL] [Abstract][Full Text] [Related]
7. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs. Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046 [TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive form of whistling face syndrome in sibs. Dallapiccola B; Giannotti A; Lembo A; Saguì L Am J Med Genet; 1989 Aug; 33(4):542-4. PubMed ID: 2596515 [TBL] [Abstract][Full Text] [Related]
9. The syndrome of multisynostotic osteodysgenesis with long-bone fractures. DeLozier CD; Antley RM; Williams R; Green N; Heller RM; Bixler D; Engel E Am J Med Genet; 1980; 7(3):391-403. PubMed ID: 7468663 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Multiple pterygium syndrome (Escobar syndrome)--a case report. Goh A; Lim KW; Rajalingam V Singapore Med J; 1994 Apr; 35(2):208-10. PubMed ID: 7939824 [TBL] [Abstract][Full Text] [Related]
16. The Pena-Shokeir syndrome: report of five cases and further delineation of the syndrome. Chen H; Blumberg B; Immken L; Lachman R; Rightmire D; Fowler M; Bachman R; Beemer FA Am J Med Genet; 1983 Oct; 16(2):213-24. PubMed ID: 6650566 [TBL] [Abstract][Full Text] [Related]
17. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant. Papadia F; Zimbalatti F; La Rosa CG Am J Med Genet; 1984 Apr; 17(4):841-7. PubMed ID: 6720749 [TBL] [Abstract][Full Text] [Related]
18. Autosomal recessive Robinow syndrome. Teebi AS Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471 [TBL] [Abstract][Full Text] [Related]
19. [Craniofacial dysostosis with diaphyseal hyperplasia]. Maximilian C; Dumitriu L; Ioanitiu D; Ispas I; Firu P; Ciovirnache M; Duca D J Genet Hum; 1981 Jun; 29(2):129-39. PubMed ID: 7328407 [TBL] [Abstract][Full Text] [Related]
20. Fountain syndrome: further delineation of the clinical syndrome and follow-up data. Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]