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.
23. Mutchinick syndrome in a Japanese girl. Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479 [TBL] [Abstract][Full Text] [Related]
24. [Smith-Lemli-Opitz syndrome: description of 2 affected brothers, clinical characterization and hereditary mechanism]. Armendares S; Carnevale A; Del Castillo V; Najar Aparicio A Rev Invest Clin; 1973; 25(2):129-42. PubMed ID: 4722228 [No Abstract] [Full Text] [Related]
25. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects. Zlotogora J; Glick B Am J Med Genet; 1993 Aug; 47(1):89-90. PubMed ID: 8368260 [TBL] [Abstract][Full Text] [Related]
26. A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment. Christian JC; Dexter RN; Palmer CG; Muller J Am J Med Genet; 1980; 6(4):301-8. PubMed ID: 6938130 [TBL] [Abstract][Full Text] [Related]
27. Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition? Stoll C; Alembik Y; Dott B Ann Genet; 1994; 37(4):207-9. PubMed ID: 7710257 [TBL] [Abstract][Full Text] [Related]
28. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome? Kotzot D; Richter K; Gierth-Fiebig K Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664 [TBL] [Abstract][Full Text] [Related]
29. A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism. Garcias Gde L; Roth Mda G Int J Neurosci; 2007 Jul; 117(7):927-33. PubMed ID: 17613106 [TBL] [Abstract][Full Text] [Related]
30. Pitt-Rogers-Danks syndrome: further delineation. Lizcano-Gil LA; García-Cruz D; García-Cruz O; Sánchez-Corona J Am J Med Genet; 1995 Feb; 55(4):420-2. PubMed ID: 7762580 [TBL] [Abstract][Full Text] [Related]
31. Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome. Mori PG; Priolo M; Lerone M; Pasino M; Caroli F; Cusano R; Seri M; Silengo MC Am J Med Genet; 1999 Nov; 87(1):36-9. PubMed ID: 10528244 [TBL] [Abstract][Full Text] [Related]
32. Filippi syndrome: report of three additional cases. Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026 [TBL] [Abstract][Full Text] [Related]
33. Clinical and genetic heterogeneity of Seckel syndrome. Faivre L; Le Merrer M; Lyonnet S; Plauchu H; Dagoneau N; Campos-Xavier AB; Attia-Sobol J; Verloes A; Munnich A; Cormier-Daire V Am J Med Genet; 2002 Nov; 112(4):379-83. PubMed ID: 12376940 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. New autosomal-recessive syndrome of Leber congenital amaurosis, short stature, growth hormone insufficiency, mental retardation, hepatic dysfunction, and metabolic acidosis. Ehara H; Nakano C; Ohno K; Goto YI; Takeshita K Am J Med Genet; 1997 Aug; 71(3):258-66. PubMed ID: 9268092 [TBL] [Abstract][Full Text] [Related]
36. Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome. Toussi T; Halal F; Lesage R; Delorme F; Bergeron A Am J Med Genet; 1980; 6(2):153-62. PubMed ID: 7446561 [TBL] [Abstract][Full Text] [Related]
38. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance. Camera G; Centa A; Pozzolo S; Camera A Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962 [TBL] [Abstract][Full Text] [Related]
39. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. Richieri-Costa A; Guion-Almeida ML; Cohen MM Am J Med Genet; 1993 Aug; 47(2):278-80. PubMed ID: 8213920 [TBL] [Abstract][Full Text] [Related]
40. Syndrome of total alopecia, multiple skeletal anomalies, shortness of stature, and mental deficiency. van Gelderen HH Am J Med Genet; 1982 Dec; 13(4):383-7. PubMed ID: 7158638 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]