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12. Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: a novel phenotype. Shah H; Bens S; Caliebe A; Graham JM; Girisha KM Am J Med Genet A; 2012 Nov; 158A(11):2941-5. PubMed ID: 22987502 [TBL] [Abstract][Full Text] [Related]
13. Melnick-Needles syndrome (osteodysplasty) in an older male--report of a case and a review of the literature. van der Lely H; Robben SG; Meradji M; Derksen-Lubsen G Br J Radiol; 1991 Sep; 64(765):852-4. PubMed ID: 1913051 [No Abstract] [Full Text] [Related]
14. Report on two cases of Freeman-Sheldon syndrome ("whistling face). Savini R; Gualdrini G Ital J Orthop Traumatol; 1980 Apr; 6(1):105-15. PubMed ID: 7203992 [TBL] [Abstract][Full Text] [Related]
15. Hunter-McAlpine syndrome: report of a third family. Adès LC; Morris LL; Simpson DA; Haan EA Clin Dysmorphol; 1993 Apr; 2(2):123-30. PubMed ID: 8281273 [TBL] [Abstract][Full Text] [Related]
16. Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome. Nishimura G; Horiuchi T; Kim OH; Sasamoto Y Am J Med Genet; 1997 Dec; 73(2):132-8. PubMed ID: 9409862 [TBL] [Abstract][Full Text] [Related]
17. Omphalocele and multiple severe congenital anomalies associated with osteodysplasty (Melnick-Needles syndrome). von Oeyen P; Holmes LB; Trelstad RL; Griscom NT Am J Med Genet; 1982 Dec; 13(4):453-63. PubMed ID: 7158644 [TBL] [Abstract][Full Text] [Related]
18. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies. Donnai D; Harris R J Med Genet; 1979 Dec; 16(6):483-6. PubMed ID: 537022 [TBL] [Abstract][Full Text] [Related]