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.
201 related articles for article (PubMed ID: 5581017)
21. Ciliary dyskinesia associated with hydrocephalus and mental retardation in a Jordanian family. al-Shroof M; Karnik AM; Karnik AA; Longshore J; Sliman NA; Khan FA Mayo Clin Proc; 2001 Dec; 76(12):1219-24. PubMed ID: 11761503 [TBL] [Abstract][Full Text] [Related]
22. Caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation: a new syndrome? Lynch SA; Lee SG; Murday VA Clin Dysmorphol; 1994 Oct; 3(4):340-6. PubMed ID: 7894739 [TBL] [Abstract][Full Text] [Related]
23. An unusual skeletal dysplasia with platyspondyly and marked digital metaphyseal involvement: a new entity? Hunter AG; Wolfish N Prog Clin Biol Res; 1982; 104():111-8. PubMed ID: 7163253 [No Abstract] [Full Text] [Related]
24. The Coffin-Lowry syndrome: an inherited faciodigital mental retardation syndrome. Temtamy SA; Miller JD; Hussels-Maumenee I J Pediatr; 1975 May; 86(5):724-31. PubMed ID: 1133653 [TBL] [Abstract][Full Text] [Related]
25. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome. Baraitser M; Winter RM J Med Genet; 1988 Jan; 25(1):41-3. PubMed ID: 3351890 [TBL] [Abstract][Full Text] [Related]
27. Parental consanguinity in two sibs with omodysplasia. Baxová A; Maroteaux P; Barosová J; Netriová I Am J Med Genet; 1994 Feb; 49(3):263-5. PubMed ID: 8209882 [TBL] [Abstract][Full Text] [Related]
28. The W syndrome. Studies of malformation syndromes of man XXVIII. Pallister PD; Herrmann J; Spranger JW; Gorlin RJ; Langer LO; Opitz JM Birth Defects Orig Artic Ser; 1974; 10(7):51-60. PubMed ID: 4425540 [No Abstract] [Full Text] [Related]
29. Radiological findings in the DOOR syndrome. Thomas PS; Nevin NC Ann Radiol (Paris); 1982 Jan; 25(1):54-8. PubMed ID: 7065610 [No Abstract] [Full Text] [Related]
30. Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome. Kohn G; Malinger G; el Shawwa R; Scheinfeld A; Tepper R; Ornoy A; Lachman R; Rimoin DL Am J Med Genet; 1995 Mar; 56(2):132-5. PubMed ID: 7625433 [TBL] [Abstract][Full Text] [Related]
32. Brachydactyly C, short stature, and hip dysplasia. Fitch N; Jequier S; Costom B Am J Med Genet; 1979; 4(2):157-66. PubMed ID: 391043 [TBL] [Abstract][Full Text] [Related]
33. Mental retardation with absent fifth fingernail and terminal phalanx. Coffin GS; Siris E Am J Dis Child; 1970 May; 119(5):433-9. PubMed ID: 5442442 [No Abstract] [Full Text] [Related]
34. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs. Toledo SP; Saldanha PH; Lamego C; Mourão PA; Dietrich CP; Mattar E Am J Med Genet; 1979; 4(3):255-61. PubMed ID: 117710 [TBL] [Abstract][Full Text] [Related]
35. A new intellectual disability syndrome with digital anomalies. Dias P; Medeira A; Cordeiro I Clin Dysmorphol; 2012 Oct; 21(4):222-225. PubMed ID: 22797554 [No Abstract] [Full Text] [Related]
36. Zimmerman-Laband syndrome and profound mental retardation. Chodirker BN; Chudley AE; Toffler MA; Reed MH Am J Med Genet; 1986 Nov; 25(3):543-7. PubMed ID: 3789014 [TBL] [Abstract][Full Text] [Related]
37. X-linked mental retardation without physical abnormality: Renpenning's syndrome. Turner G; Turner B; Collins E Dev Med Child Neurol; 1971 Feb; 13(1):71-8. PubMed ID: 4929082 [No Abstract] [Full Text] [Related]
38. Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus. Fried K; Sanger R J Med Genet; 1973 Mar; 10(1):17-8. PubMed ID: 4697849 [TBL] [Abstract][Full Text] [Related]
39. Poland's syndrome with radial aplasia of the hand. De Smet L Genet Couns; 2013; 24(1):57-9. PubMed ID: 23610865 [TBL] [Abstract][Full Text] [Related]