These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
117 related articles for article (PubMed ID: 953243)
21. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia. Cunniff C; Jones KL; Saal HM; Stern HJ Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962 [TBL] [Abstract][Full Text] [Related]
22. Amniotic band syndrome with significant orofacial clefts and disruptions and distortions of craniofacial structures. Muraskas JK; McDonnell JF; Chudik RJ; Salyer KE; Glynn L J Pediatr Surg; 2003 Apr; 38(4):635-8. PubMed ID: 12677585 [TBL] [Abstract][Full Text] [Related]
23. Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment. Grubben C; Fryns JP; De Zegher F; Van Den Berghe H Genet Couns; 1990; 1(2):103-9. PubMed ID: 2080994 [TBL] [Abstract][Full Text] [Related]
24. Trisomy 4p in a family with A t(4;15). Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034 [TBL] [Abstract][Full Text] [Related]
25. BBBG syndrome or Opitz syndrome: new family. Verloes A; Le Merrer M; Briard ML Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419 [TBL] [Abstract][Full Text] [Related]
26. New syndrome in three affected siblings. Crane JP; Heise RL Pediatrics; 1981 Aug; 68(2):235-7. PubMed ID: 7267231 [TBL] [Abstract][Full Text] [Related]
27. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis. Toriello HV; Higgins JV Am J Med Genet; 1995 Jan; 55(2):200-4. PubMed ID: 7717418 [TBL] [Abstract][Full Text] [Related]
29. Ocular manifestations in Delleman syndrome (Oculocerebrocutaneous syndrome, OCC-syndrome) and encephalocraniocutaneous lipomatosis (ECCL). Report of three cases. Narbay G; Meire F; Verloes A; Casteels I; Devos E Bull Soc Belge Ophtalmol; 1996; 261():65-70. PubMed ID: 9009364 [TBL] [Abstract][Full Text] [Related]
30. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature. Gollop TR; Fontes LR Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752 [TBL] [Abstract][Full Text] [Related]
31. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome. Goddeeris P; Fryns JP; van den Berghe H J Genet Hum; 1980 Mar; 28(1):57-60. PubMed ID: 7400786 [TBL] [Abstract][Full Text] [Related]
32. Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins. Cleper R; Kauschansky A; Varsano I; Frydman M Am J Med Genet; 1993 Sep; 47(4):451-5. PubMed ID: 8256802 [TBL] [Abstract][Full Text] [Related]
33. Craniofacial morphology in the velo-cardio-facial syndrome. Arvystas M; Shprintzen RJ J Craniofac Genet Dev Biol; 1984; 4(1):39-45. PubMed ID: 6736220 [TBL] [Abstract][Full Text] [Related]
35. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings. Neu RL; Kajii T; Gardner LI; Nagyfy SF Pediatrics; 1971 Mar; 47(3):610-2. PubMed ID: 5547878 [No Abstract] [Full Text] [Related]