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3. Slowly progressive macrocephaly with hamartomas: a new syndrome? Halal F; Silver K Am J Med Genet; 1989 Jun; 33(2):182-5. PubMed ID: 2764028 [TBL] [Abstract][Full Text] [Related]
5. [Macrocephaly and multiple hemangiomas in two brothers]. Martinón Sánchez F; Pérez Gómez E; García Rodríguez JL An Esp Pediatr; 1991 Jun; 34(6):475-6. PubMed ID: 1929019 [No Abstract] [Full Text] [Related]
6. Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Hsia YE; Bratu M; Herbordt A Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860 [No Abstract] [Full Text] [Related]
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8. Hemimegalencephaly and linear nevus sebaceous syndrome. Herman TE; Siegel MJ J Perinatol; 2001; 21(5):336-8. PubMed ID: 11536031 [No Abstract] [Full Text] [Related]
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10. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Kang S; Graham JM; Olney AH; Biesecker LG Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938 [TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E; Palmieri A; Bertola A; Bellini C Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417 [TBL] [Abstract][Full Text] [Related]
12. Varadi syndrome or Opitz trigonocephaly: overlapping manifestation in two cousins. Bankier A; Rose CM Am J Med Genet; 1994 Oct; 53(1):85-8. PubMed ID: 7802045 [No Abstract] [Full Text] [Related]
13. Polydactyly in a carrier of the gene for the Meckel syndrome. Nelson J; Nevin NC; Hanna EJ Am J Med Genet; 1994 Nov; 53(3):207-9. PubMed ID: 7856653 [TBL] [Abstract][Full Text] [Related]
15. The Meckel syndrome in Finland: epidemiologic and genetic aspects. Salonen R; Norio R Am J Med Genet; 1984 Aug; 18(4):691-8. PubMed ID: 6486168 [TBL] [Abstract][Full Text] [Related]
16. Familial Pallister-Hall syndrome: case report and hormonal evaluation. Sills IN; Rapaport R; Robinson LP; Lieber C; Shih LY; Horlick MN; Schwartz M; Desposito F Am J Med Genet; 1993 Sep; 47(3):321-5. PubMed ID: 8135274 [TBL] [Abstract][Full Text] [Related]
17. [Hydrometrocolpos, polydactylia and congenital heart defect (the McKusick-Dungy-Kaufman syndrome)]. Hamel BC; ter Haar BG Tijdschr Kindergeneeskd; 1984 Aug; 52(4):129-33. PubMed ID: 6495304 [TBL] [Abstract][Full Text] [Related]