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5. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance. Corsello G; Giuffrè L Am J Med Genet; 1994 Jan; 49(1):137-8. PubMed ID: 8172244 [No Abstract] [Full Text] [Related]
6. Postmortem findings in three triploid fetuses. de Ravel TJ; Wright CA; Moller LI Birth Defects Orig Artic Ser; 1996; 30(1):341-52. PubMed ID: 9125338 [No Abstract] [Full Text] [Related]
7. The Dubowitz syndrome. Wilroy RS; Tipton RE; Summitt RL Am J Med Genet; 1978; 2(3):275-84. PubMed ID: 263660 [TBL] [Abstract][Full Text] [Related]
8. US case of the day. Pena-Shokeir phenotype. Horrow MM; Rosenberg HK; Schneider AS; Greenberg CM; Zaeri N Radiographics; 1995 May; 15(3):726-9. PubMed ID: 7624577 [No Abstract] [Full Text] [Related]
9. [Hydrocephalus in one twin after massive reverse flow in the umbilical artery in the 2nd trimester]. Erz W; Gonser M; Vochem M Geburtshilfe Frauenheilkd; 1994 Aug; 54(8):471-4. PubMed ID: 7982553 [TBL] [Abstract][Full Text] [Related]
10. Extreme intrauterine growth retardation, hydrocephalus and aged facial appearance: a previously unrecognized autosomal recessive disorder? Winter RM; Shortland D; Collins AL; Hall CM; Temple IK Clin Dysmorphol; 1996 Oct; 5(4):313-9. PubMed ID: 8905196 [TBL] [Abstract][Full Text] [Related]
11. New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia. Giampietro PF; Auerbach AD; Elias ER; Gutman A; Zellers NJ; Davis JG Am J Med Genet; 1998 Jun; 78(1):70-5. PubMed ID: 9637428 [TBL] [Abstract][Full Text] [Related]
12. The Neu-Laxova syndrome: comments on syndrome identification. Fitch N; Resch L; Rochon L Am J Med Genet; 1982 Dec; 13(4):445-52. PubMed ID: 6891564 [No Abstract] [Full Text] [Related]
13. Intrauterine growth retardation, duodenal and extrahepatic biliary atresia, hypoplastic pancreas and other intestinal anomalies: further evidence of the Martínez-Frías syndrome. Galán-Gómez E; Sánchez EB; Arias-Castro S; Cardesa-García JJ Eur J Med Genet; 2007; 50(2):144-8. PubMed ID: 17321227 [TBL] [Abstract][Full Text] [Related]
14. A case of ring chromosome 13 with ambiguous genitalia and primary hypothyroidism. Sandal G; Caliskan D; Ormeci AR; Oztas S Genet Couns; 2012; 23(4):529-32. PubMed ID: 23431756 [No Abstract] [Full Text] [Related]
15. 69,XXX karyotype in a malformed liveborn female. Maternal origin of triploidy. Galán F; Orts F; Aguilar MS; Clemente F; Loeda C; Aranda I; Jimenez Cobo B Ann Genet; 1991; 34(1):37-9. PubMed ID: 1952791 [TBL] [Abstract][Full Text] [Related]
17. Walker-Warburg syndrome: report of three affected sibs. Rodgers BL; Vanner LV; Pai GS; Sens MA Am J Med Genet; 1994 Jan; 49(2):198-201. PubMed ID: 8116667 [TBL] [Abstract][Full Text] [Related]
18. Perinatal imaging findings of Galloway-Mowat syndrome. Chen CP; Lin SP; Tsai JD; Huang JK; Yen JL; Tseng CC; Wang W Genet Couns; 2007; 18(3):353-5. PubMed ID: 18019379 [No Abstract] [Full Text] [Related]
19. Etiologic complexities of diaphragmatic defects: right diaphragmatic hernia, pulmonary hypoplasia/agenesis, and hydrocephalus in sibs. Bieber FR; Dawson AE; Holmes LB Am J Med Genet; 1991 Nov; 41(2):164-8. PubMed ID: 1723847 [TBL] [Abstract][Full Text] [Related]
20. Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients. Arboleda H; Quintero L; Yunis E J Med Genet; 1997 May; 34(5):433-7. PubMed ID: 9152846 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]