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.
22. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes. Dincsoy MY; Salih MA; al-Jurayyan N; al Saadi M; Patel PJ Am J Med Genet; 1995 Apr; 56(3):317-21. PubMed ID: 7778599 [TBL] [Abstract][Full Text] [Related]
25. Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome. ter Heide H; Bulstra SK; Reekers A; Schrander JJ; Schrander-Stumpel CT Am J Med Genet; 2002 Jul; 110(4):359-64. PubMed ID: 12116210 [TBL] [Abstract][Full Text] [Related]
26. Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association. Twede JV; Difazio M Pediatr Dermatol; 2009; 26(1):97-9. PubMed ID: 19250421 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. Oral-facial-skeletal syndromes. Neri G; Gurrieri F; Genuardi M Am J Med Genet; 1995 Nov; 59(3):365-8. PubMed ID: 8599363 [No Abstract] [Full Text] [Related]
29. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240 [TBL] [Abstract][Full Text] [Related]
30. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome? Moog U; Bleeker-Wagemakers EM; Crobach P; Vles JS; Schrander-Stumpel CT Am J Med Genet; 1998 Jul; 78(3):263-6. PubMed ID: 9677063 [TBL] [Abstract][Full Text] [Related]
31. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies. Jonas RE; Kimonis VE; Morales A Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870 [TBL] [Abstract][Full Text] [Related]
32. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome. al-Gazali LI; Bakir M; Sadaghatian MR; Nath R; Haas D Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196 [TBL] [Abstract][Full Text] [Related]
33. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome. Kantaputra PN; Kunachaichote J; Patikulsila P Am J Med Genet; 2001 Nov; 103(4):283-8. PubMed ID: 11746007 [TBL] [Abstract][Full Text] [Related]
34. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant. Papadia F; Zimbalatti F; La Rosa CG Am J Med Genet; 1984 Apr; 17(4):841-7. PubMed ID: 6720749 [TBL] [Abstract][Full Text] [Related]
35. Another case of the autosomal recessive Weaver-like syndrome. Slaney SF; Winter RM Am J Med Genet; 1997 Oct; 72(3):369-70. PubMed ID: 9332672 [No Abstract] [Full Text] [Related]
36. 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]
37. Caroline Crachami, the Sicilian fairy: a further note. Bondeson J Am J Med Genet; 1993 Jun; 46(4):471. PubMed ID: 8357026 [No Abstract] [Full Text] [Related]
38. Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters. Knoblauch H; Urban M; Tinschert S Genet Couns; 1999; 10(3):315-20. PubMed ID: 10546105 [TBL] [Abstract][Full Text] [Related]