102 related articles for article (PubMed ID: 1684092)
1. Smith-Fineman-Myers syndrome in two brothers.
Adès LC; Kerr B; Turner G; Wise G
Am J Med Genet; 1991 Sep; 40(4):467-70. PubMed ID: 1684092
[TBL] [Abstract][Full Text] [Related]
2. [Mapping the gene responsible for Smith-Fineman-Myers syndrome to Xq25].
Gong Y; Wei J; Shao C; Guo Y; Chen B; Guo C; Warman M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):277-80. PubMed ID: 10514530
[TBL] [Abstract][Full Text] [Related]
3. Smith-Fineman-Myers syndrome: report on a large family.
Wei J; Chen B; Jiang Y; Yang Y; Guo Y
Am J Med Genet; 1993 Sep; 47(3):307-11. PubMed ID: 8135271
[TBL] [Abstract][Full Text] [Related]
4. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
Chudley AE; Lowry RB; Hoar DI
Am J Med Genet; 1988 Dec; 31(4):741-51. PubMed ID: 3239563
[TBL] [Abstract][Full Text] [Related]
5. Smith-Fineman-Myers syndrome: report of a third case.
Stephenson LD; Johnson JP
Am J Med Genet; 1985 Oct; 22(2):301-4. PubMed ID: 4050861
[TBL] [Abstract][Full Text] [Related]
6. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
Brooks SS; Wisniewski K; Brown WT
Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
[TBL] [Abstract][Full Text] [Related]
7. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
[TBL] [Abstract][Full Text] [Related]
8. [Linkage analysis and mutation detection of GRIA3 in Smith--Fineman--Myers syndrome].
Liu QJ; Gong YQ; Chen BX; Guo CH; Li JX; Guo YS
Yi Chuan Xue Bao; 2001 Nov; 28(11):985-90. PubMed ID: 11725645
[TBL] [Abstract][Full Text] [Related]
9. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
Riccardi VM; Hässler E; Lubinsky MS
Am J Med Genet; 1977; 1(1):47-58. PubMed ID: 565138
[TBL] [Abstract][Full Text] [Related]
10. New X-linked syndrome of mental retardation, short stature, and hypertelorism.
Stoll C; Géraudel A; Chauvin A
Am J Med Genet; 1991 Jun; 39(4):474-8. PubMed ID: 1877628
[TBL] [Abstract][Full Text] [Related]
11. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
Bottani A; Schinzel A
Clin Dysmorphol; 1993 Jul; 2(3):225-31. PubMed ID: 8287184
[TBL] [Abstract][Full Text] [Related]
12. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
Bindewald B; Ulmer H; Müller U
Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
[TBL] [Abstract][Full Text] [Related]
13. The craniodigital syndrome of Scott: report of a second family.
Lorenz P; Hinkel GK; Hoffmann C; Rupprecht E
Am J Med Genet; 1990 Oct; 37(2):224-6. PubMed ID: 2174209
[TBL] [Abstract][Full Text] [Related]
14. Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?
Saugier-Veber P; Munnich A; Lyonnet S; Toutain A; Moraine C; Piussan C; Mathieu M; Gibbons RJ
Am J Med Genet; 1995 Jan; 55(3):300-1. PubMed ID: 7726226
[No Abstract] [Full Text] [Related]
15. 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]
16. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
Wittwer B; Kircheisen R; Leutelt J; Orth U; Gal A
Am J Med Genet; 1996 Jul; 64(1):42-9. PubMed ID: 8826447
[TBL] [Abstract][Full Text] [Related]
17. FG syndrome: report of three new families with linkage to Xq12-q22.1.
Graham JM; Tackels D; Dibbern K; Superneau D; Rogers C; Corning K; Schwartz CE
Am J Med Genet; 1998 Nov; 80(2):145-56. PubMed ID: 9805132
[TBL] [Abstract][Full Text] [Related]
18. X-linked syndrome of mental retardation, short stature, and hypertelorism: a new syndrome or a further example of the FG syndrome?
Bottani A
Am J Med Genet; 1994 May; 51(1):87-8. PubMed ID: 8030678
[No Abstract] [Full Text] [Related]
19. New syndrome or severe expression of Gordon syndrome? A case report.
Courtens W; Perlmutter N; Dan B; Vamos E
Clin Dysmorphol; 1997 Jan; 6(1):39-44. PubMed ID: 9018417
[TBL] [Abstract][Full Text] [Related]
20. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
Lungarotti MS; Martello C; Barboni G; Mezzetti D; Mariotti G; Calabro A
Am J Med Genet; 1994 Jul; 51(4):598-601. PubMed ID: 7943046
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
