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22. Dominantly inherited syndrome of microcephaly and cleft palate. Halal F Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112 [TBL] [Abstract][Full Text] [Related]
23. [3 children with velocardiofacial (Shprintzen) syndrome]. Lie DA; Beemer FA Ned Tijdschr Geneeskd; 1996 Feb; 140(7):372-5. PubMed ID: 8628424 [TBL] [Abstract][Full Text] [Related]
24. Autosomal dominant inheritance of the Aarskog syndrome. Grier RE; Farrington FH; Kendig R; Mamunes P Am J Med Genet; 1983 May; 15(1):39-46. PubMed ID: 6344635 [TBL] [Abstract][Full Text] [Related]
25. Anal atresia and abdominal wall defect as unusual symptoms in EEC syndrome. De Smet L; Fryns JP Genet Couns; 1995; 6(2):127-30. PubMed ID: 7546455 [TBL] [Abstract][Full Text] [Related]
32. New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects. Middleton LT; Anastasiades V; Panayidou K; Georghiou D; Kalli E; Gabriel G; Myrianthopoulos NC Am J Med Genet; 1992 Dec; 44(6):757-61. PubMed ID: 1481843 [TBL] [Abstract][Full Text] [Related]
33. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation. Tsukahara M; Sugio Y J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671 [TBL] [Abstract][Full Text] [Related]
34. New evidence for genetic heterogeneity of the Freeman-Sheldon syndrome. Sánchez JM; Kaminker CP Am J Med Genet; 1986 Nov; 25(3):507-11. PubMed ID: 3789012 [TBL] [Abstract][Full Text] [Related]
35. Dominant inheritance of syn-camptodactyly of the second and third toes with foot and lower limb asymmetry and scoliosis. Halal F Am J Med Genet; 1985 Sep; 22(1):149-56. PubMed ID: 4050850 [TBL] [Abstract][Full Text] [Related]
37. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2. Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665 [TBL] [Abstract][Full Text] [Related]
38. New syndrome: progressive scoliosis by unilateral unsegmented fusion bar, foot deformity, joint laxity, congenital inguinal herniae, peculiar face. Ventruto V; Catani L Am J Med Genet; 1986 Nov; 25(3):429-32. PubMed ID: 3789006 [No Abstract] [Full Text] [Related]
39. A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly. Rozin MM; Hertz M; Goodman RM Clin Genet; 1984 Oct; 26(4):342-55. PubMed ID: 6437708 [TBL] [Abstract][Full Text] [Related]
40. Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome? Fryns JP; Smeets E; Thiry P; Geutjens J; Vinken L; Van den Berghe H Am J Med Genet; 1994 Jan; 49(1):91-3. PubMed ID: 8172258 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]