836 related articles for article (PubMed ID: 10533026)
21. GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome.
Verloes A; Delfortrie J; Lambotte C
Am J Med Genet; 1989 Jan; 32(1):15-8. PubMed ID: 2705477
[No Abstract] [Full Text] [Related]
22. Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.
Clemens M; Martsolf JT; Rogers JG; Mowery-Rushton P; Surti U; McPherson E
Am J Med Genet; 1996 Dec; 66(1):95-100. PubMed ID: 8957524
[TBL] [Abstract][Full Text] [Related]
23. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
[TBL] [Abstract][Full Text] [Related]
24. The Dubowitz syndrome--one more case.
Chrzanowska KH; Krajewska-Walasek M
Klin Padiatr; 1987; 199(5):370-2. PubMed ID: 3316825
[TBL] [Abstract][Full Text] [Related]
25. Autosomal recessive microcephaly with severe psychomotor retardation.
Scheffer IE; Baraitser M; Wilson J; Godfrey C; Brett EM
Neuropediatrics; 1992 Feb; 23(1):53-6. PubMed ID: 1565220
[TBL] [Abstract][Full Text] [Related]
26. Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.
Cooperstone BG; Friedman A; Kaplan BS
Am J Med Genet; 1993 Aug; 47(2):250-4. PubMed ID: 8213914
[TBL] [Abstract][Full Text] [Related]
27. Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.
Woods CG; Crouchman M; Huson SM
J Med Genet; 1992 Jul; 29(7):500-2. PubMed ID: 1640433
[TBL] [Abstract][Full Text] [Related]
28. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
[TBL] [Abstract][Full Text] [Related]
29. Filippi syndrome: a new case with skeletal abnormalities.
Héron D; Billette de Villemeur T; Munnich A; Lyonnet S
J Med Genet; 1995 Aug; 32(8):659-61. PubMed ID: 7473664
[TBL] [Abstract][Full Text] [Related]
30. A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency.
Bouwes Bavinck JN; Weaver DD; Ellis FD; Ward RE
Am J Med Genet; 1987 Apr; 26(4):825-31. PubMed ID: 3109242
[TBL] [Abstract][Full Text] [Related]
31. [Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies].
Castro-Gago M; Pombo M; Novo I; Tojo R; Peña J
An Esp Pediatr; 1983 Aug; 19(2):128-31. PubMed ID: 6660641
[TBL] [Abstract][Full Text] [Related]
32. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
[TBL] [Abstract][Full Text] [Related]
33. Multiple dental and skeletal abnormalities in an individual with filippi syndrome.
Sandhu M; Malik P; Saha R
Case Rep Dent; 2013; 2013():845405. PubMed ID: 24222867
[TBL] [Abstract][Full Text] [Related]
34. Tapetoretinal degeneration and mental retardation associated with microspherophakia and mesodermal abnormalities: a new syndrome?
Sierpinski-Bart J; Neumann E; Tirosh E; Atias D
Metab Pediatr Ophthalmol; 1981; 5(3-4):225-31. PubMed ID: 6273671
[No Abstract] [Full Text] [Related]
35. Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome.
Doerfler W; Wieczorek D; Gillessen-Kaesbach G; Albrecht B; Passarge E
Am J Med Genet; 1997 Dec; 73(2):210-6. PubMed ID: 9409875
[TBL] [Abstract][Full Text] [Related]
36. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
Nakata NM; Guion-Almeida ML; Richieri-Costa A
Am J Med Genet; 1993 Sep; 47(3):330-2. PubMed ID: 8135276
[TBL] [Abstract][Full Text] [Related]
37. Dominantly inherited syndrome of microcephaly and cleft palate.
Halal F
Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
[TBL] [Abstract][Full Text] [Related]
38. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
Schinzel A; Schmid W
Am J Med Genet; 1980; 6(3):241-9. PubMed ID: 7424976
[TBL] [Abstract][Full Text] [Related]
39. Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndrome.
Collignon P; Philip N; Simonin G; Mattei JF; Giraud F
Genet Couns; 1992; 3(4):221-2. PubMed ID: 1472358
[TBL] [Abstract][Full Text] [Related]
40. A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
Schimke RN; Horton WA; Collins DL; Therou L
Am J Med Genet; 1984 Jan; 17(1):323-32. PubMed ID: 6538752
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]