103 related articles for article (PubMed ID: 8357010)
41. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
Tsukahara M; Sugio Y
J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
[TBL] [Abstract][Full Text] [Related]
42. X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndrome.
Morava E; Storcz J; Kosztolányi G
Am J Med Genet; 1996 Jul; 64(1):59-62. PubMed ID: 8826449
[TBL] [Abstract][Full Text] [Related]
43. The KBG syndrome: an additional sporadic case.
Mathieu M; Helou M; Morin G; Dolhem P; Devauchelle B; Piussan C
Genet Couns; 2000; 11(1):33-5. PubMed ID: 10756425
[TBL] [Abstract][Full Text] [Related]
44. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
[TBL] [Abstract][Full Text] [Related]
45. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies. A new syndrome?
Guion-Almeida ML; Richieri-Costa A
Clin Dysmorphol; 1999 Jan; 8(1):1-4. PubMed ID: 10327243
[TBL] [Abstract][Full Text] [Related]
46. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
Terespolsky D; Farrell SA; Siegel-Bartelt J; Weksberg R
Am J Med Genet; 1995 Nov; 59(3):329-33. PubMed ID: 8599356
[TBL] [Abstract][Full Text] [Related]
47. Toriello-Carey syndrome: evidence for X-linked inheritance.
Czarnecki P; Lacombe D; Weiss L
Am J Med Genet; 1996 Nov; 65(4):291-4. PubMed ID: 8923938
[TBL] [Abstract][Full Text] [Related]
48. Craniotubular dysplasia with severe postnatal growth retardation, mental retardation, ectodermal dysplasia, and loose skin: Lenz-Majewski-like syndrome.
Nishimura G; Harigaya A; Kuwashima M; Kuwashima S
Am J Med Genet; 1997 Jul; 71(1):87-92. PubMed ID: 9215775
[TBL] [Abstract][Full Text] [Related]
49. New syndrome?: MCA/MR syndrome with multiple circumferential skin creases.
Elliott AM; Ludman M; Teebi AS
Am J Med Genet; 1996 Mar; 62(1):23-5. PubMed ID: 8779319
[TBL] [Abstract][Full Text] [Related]
50. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
Seemanová E; Lesný I
Am J Med Genet; 1996 Dec; 66(2):179-83. PubMed ID: 8958326
[TBL] [Abstract][Full Text] [Related]
51. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
52. Kabuki Syndrome with additional dental findings: a case report.
Cogulu D; Oncag O; Celen E; Ozkinay F
J Dent Child (Chic); 2008; 75(2):185-7. PubMed ID: 18647516
[TBL] [Abstract][Full Text] [Related]
53. 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]
54. An aminopterin-like syndrome without aminopterin (ASSAS).
Fraser FC; Anderson RA; Mulvihill JI; Preus M
Clin Genet; 1987 Jul; 32(1):28-34. PubMed ID: 3621652
[TBL] [Abstract][Full Text] [Related]
55. Picture of the month. Aminopterin embryopathy syndrome.
Gellis SS; Feingold M
Am J Dis Child; 1979 Nov; 133(11):1189-90. PubMed ID: 507011
[No Abstract] [Full Text] [Related]
56. King-Denborough Syndrome: report of two Brazilian cases.
Reed UC; Resende MB; Ferreira LG; Carvalho MS; Diament A; Scaff M; Marie SK
Arq Neuropsiquiatr; 2002 Sep; 60(3-B):739-41. PubMed ID: 12364941
[TBL] [Abstract][Full Text] [Related]
57. Etiopathogenesis of craniosynostosis.
Cohen MM
Neurosurg Clin N Am; 1991 Jul; 2(3):507-13. PubMed ID: 1821298
[TBL] [Abstract][Full Text] [Related]
58. Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency.
Kingston HM; Hughes IA; Harper PS
Arch Dis Child; 1982 Oct; 57(10):790-2. PubMed ID: 7138070
[TBL] [Abstract][Full Text] [Related]
59. THE PURIFICATION OF AMINOPTERIN.
LOO TL
J Med Chem; 1965 Jan; 8():139. PubMed ID: 14287252
[No Abstract] [Full Text] [Related]
60. [Effect of aminopterin in rat].
LEWIS JT; RABASA SL; FERRER J; DOMENICO AD
Sang; 1953; 24(7):599-600. PubMed ID: 13135376
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]