232 related articles for article (PubMed ID: 7645599)
1. Autosomal dominant inheritance in Setleis syndrome.
Masuno M; Imaizumi K; Makita Y; Nakamura M; Kuroki Y
Am J Med Genet; 1995 May; 57(1):57-60. PubMed ID: 7645599
[TBL] [Abstract][Full Text] [Related]
2. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance.
Artlich A; Schwinger E; Meinecke P
Clin Dysmorphol; 1992 Jul; 1(3):157-60. PubMed ID: 1342863
[TBL] [Abstract][Full Text] [Related]
3. Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
al-Gazali LI; al-Talabani J
Clin Dysmorphol; 1996 Jul; 5(3):249-53. PubMed ID: 8818454
[TBL] [Abstract][Full Text] [Related]
4. Setleis syndrome: three new cases and a review of the literature.
McGaughran J; Aftimos S
Am J Med Genet; 2002 Sep; 111(4):376-80. PubMed ID: 12210295
[TBL] [Abstract][Full Text] [Related]
5. Expanded phenotype and ethnicity in Setleis syndrome.
Clark RD; Golabi M; Lacassie Y; Hall B; Seto S
Am J Med Genet; 1989 Nov; 34(3):354-7. PubMed ID: 2596524
[TBL] [Abstract][Full Text] [Related]
6. Ruvalcaba syndrome: autosomal dominant inheritance.
Sugio Y; Kajii T
Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
[TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant inheritance in a large family with focal facial dermal dysplasia (Brauer-Setleis syndrome).
Graul-Neumann LM; Stieler KM; Blume-Peytavi U; Tzschach A
Am J Med Genet A; 2009 Feb; 149A(4):746-50. PubMed ID: 19291768
[TBL] [Abstract][Full Text] [Related]
8. Evidence for genetic homogeneity of Setleis' syndrome and focal facial dermal dysplasia.
Ward KA; Moss C
Br J Dermatol; 1994 May; 130(5):645-9. PubMed ID: 8204474
[TBL] [Abstract][Full Text] [Related]
9. Ophthalmic findings in Setleis syndrome: two new cases in a mother and son.
Kent JS; Romanchuk KG; Lemire EG
Can J Ophthalmol; 2007 Jun; 42(3):471-3. PubMed ID: 17508049
[TBL] [Abstract][Full Text] [Related]
10. Follow-up study in a patient with Setleis syndrome.
Tsukahara M; Okabe T; Ohtsuka M; Furukawa S
Am J Med Genet; 1995 Jul; 57(3):444-6. PubMed ID: 7677148
[TBL] [Abstract][Full Text] [Related]
11. Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification.
Cervantes-Barragán DE; Villarroel CE; Medrano-Hernández A; Durán-McKinster C; Bosch-Canto V; Del-Castillo V; Nazarenko I; Yang A; Desnick RJ
J Med Genet; 2011 Oct; 48(10):716-20. PubMed ID: 21931173
[TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant inheritance of the DeMyer Sequence.
Jaramillo C; Brandt SK; Jorgenson RJ
J Craniofac Genet Dev Biol; 1988; 8(3):199-204. PubMed ID: 3209682
[TBL] [Abstract][Full Text] [Related]
13. Setleis ('bitemporal forceps marks') syndrome.
Garcia-Minaur S; Linares A
Clin Dysmorphol; 1995 Apr; 4(2):173-5. PubMed ID: 7606326
[No Abstract] [Full Text] [Related]
14. Williams syndrome: autosomal dominant inheritance.
Morris CA; Thomas IT; Greenberg F
Am J Med Genet; 1993 Sep; 47(4):478-81. PubMed ID: 8256809
[TBL] [Abstract][Full Text] [Related]
15. Autosomal recessive inheritance in the Setleis bitemporal 'forceps marks' syndrome.
Marion RW; Chitayat D; Hutcheon RG; Goldberg R; Shprintzen RJ; Cohen MM
Am J Dis Child; 1987 Aug; 141(8):895-7. PubMed ID: 3631024
[TBL] [Abstract][Full Text] [Related]
16. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J
Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
[TBL] [Abstract][Full Text] [Related]
17. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance.
Hordijk R; Van de Logt F; Houtman WA; Van Essen AJ
Genet Couns; 1996; 7(2):113-22. PubMed ID: 8831130
[TBL] [Abstract][Full Text] [Related]
18. Genetics of the Costello syndrome.
Lurie IW
Am J Med Genet; 1994 Sep; 52(3):358-9. PubMed ID: 7528974
[TBL] [Abstract][Full Text] [Related]
19. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
Teebi AS
Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
[TBL] [Abstract][Full Text] [Related]
20. Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters.
Knoblauch H; Urban M; Tinschert S
Genet Couns; 1999; 10(3):315-20. PubMed ID: 10546105
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]