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3. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot. Jones MC; Waldman JD Am J Med Genet; 1985 Sep; 22(1):135-41. PubMed ID: 4050848 [TBL] [Abstract][Full Text] [Related]
4. Male-to-male transmission of the velo-cardio-facial syndrome: a case report and review of 60 cases. Williams MA; Shprintzen RJ; Goldberg RB J Craniofac Genet Dev Biol; 1985; 5(2):175-80. PubMed ID: 4019731 [TBL] [Abstract][Full Text] [Related]
5. Velo-cardio-facial syndrome: a review of 120 patients. Goldberg R; Motzkin B; Marion R; Scambler PJ; Shprintzen RJ Am J Med Genet; 1993 Feb; 45(3):313-9. PubMed ID: 8434617 [TBL] [Abstract][Full Text] [Related]
12. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot]. Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712 [TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant inheritance of the DeMyer Sequence. Jaramillo C; Brandt SK; Jorgenson RJ J Craniofac Genet Dev Biol; 1988; 8(3):199-204. PubMed ID: 3209682 [TBL] [Abstract][Full Text] [Related]
15. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions. Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167 [TBL] [Abstract][Full Text] [Related]
16. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly. Martin NJ; Steinberg BG Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406 [TBL] [Abstract][Full Text] [Related]
17. Jones-Waldman syndrome: another report? Schuler L; Puga AC; Schwartz IV; Netto C Am J Med Genet; 1994 May; 51(1):83. PubMed ID: 8030675 [No Abstract] [Full Text] [Related]
18. Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype. McLean SD; Saal HM; Spinner NB; Emanuel BS; Driscoll DA Am J Dis Child; 1993 Nov; 147(11):1212-6. PubMed ID: 8237917 [TBL] [Abstract][Full Text] [Related]
19. Misclassification risk of patients with bilateral cleft lip and palate and manifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome? Schulze BR; Tariverdian G; Komposch G; Stellzig A Am J Med Genet; 2001 Apr; 99(4):280-5. PubMed ID: 11251993 [TBL] [Abstract][Full Text] [Related]
20. An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly. Martin AO; Perrin JC; Muir WA; Ruch E; Schafer IA Clin Genet; 1977 Aug; 12(2):65-72. PubMed ID: 891015 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]