158 related articles for article (PubMed ID: 11102936)
1. Blaschkolinear skin pigmentary variation due to trisomy 7 mosaicism.
Kayser M; Henderson LB; Kreutzman J; Schreck R; Graham JM
Am J Med Genet; 2000 Nov; 95(3):281-4. PubMed ID: 11102936
[TBL] [Abstract][Full Text] [Related]
2. Prenatally detected trisomy 7 mosaicism in a dysmorphic child.
Kivirikko S; Salonen R; Salo A; von Koskull H
Prenat Diagn; 2002 Jul; 22(7):541-4. PubMed ID: 12124684
[TBL] [Abstract][Full Text] [Related]
3. Phylloid hypomelanosis is closely related to mosaic trisomy 13.
Happle R
Eur J Dermatol; 2000; 10(7):511-2. PubMed ID: 11056419
[TBL] [Abstract][Full Text] [Related]
4. Mosaic trisomy 7 in a patient with pigmentary abnormalities.
Verghese S; Newlin A; Miller M; Burton BK
Am J Med Genet; 1999 Dec; 87(5):371-4. PubMed ID: 10594873
[TBL] [Abstract][Full Text] [Related]
5. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes.
Taibjee SM; Hall D; Balderson D; Larkins S; Stubbs T; Moss C
Clin Exp Dermatol; 2009 Oct; 34(7):823-9. PubMed ID: 19438553
[TBL] [Abstract][Full Text] [Related]
6. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
[TBL] [Abstract][Full Text] [Related]
7. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
Font-Montgomery E; Stone KM; Weaver DD; Vance GH; Das S; Thurston VC
Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):577-82. PubMed ID: 16007591
[TBL] [Abstract][Full Text] [Related]
8. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
Flori E; Girodon E; Samama B; Becmeur F; Viville B; Girard-Lemaire F; Doray B; Schluth C; Marcellin L; Boehm N; Goossens M; Pingault V
Eur J Hum Genet; 2005 Sep; 13(9):1013-8. PubMed ID: 15915162
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.
Merritt TA; Natarajan G
Am J Perinatol; 2007 Oct; 24(9):563-6. PubMed ID: 17893842
[TBL] [Abstract][Full Text] [Related]
10. Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.
González-Enseñat MA; Vicente A; Poo P; Catalá V; Mar Pérez-Iribarne M; Fuster C; Geán E; Happle R
Arch Dermatol; 2009 May; 145(5):576-8. PubMed ID: 19451503
[TBL] [Abstract][Full Text] [Related]
11. Mosaic trisomy 14 with hepatic involvement.
Iglesias A; McCurdy LD; Glass IA; Cotter PD; Illueca M; Perenyi A; Sansaricq C
Ann Genet; 1997; 40(2):104-8. PubMed ID: 9259957
[TBL] [Abstract][Full Text] [Related]
12. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
Langlois S; Yong PJ; Yong SL; Barrett I; Kalousek DK; Miny P; Exeler R; Morris K; Robinson WP
Prenat Diagn; 2006 Jun; 26(6):548-58. PubMed ID: 16683298
[TBL] [Abstract][Full Text] [Related]
13. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
Fogu G; Maserati E; Cambosu F; Moro MA; Poddie F; Soro G; Bandiera P; Serra G; Tusacciu G; Sanna G; Mazzarello V; Montella A
Eur J Med Genet; 2008; 51(4):303-14. PubMed ID: 18495567
[TBL] [Abstract][Full Text] [Related]
14. Delineation of a clinical syndrome caused by mosaic trisomy 15.
Bühler EM; Bienz G; Straumann E; Bösch N
Am J Med Genet; 1996 Mar; 62(2):109-12. PubMed ID: 8882390
[TBL] [Abstract][Full Text] [Related]
15. An unusual human mosaic for skin pigmentation.
Stoll C; Alembik Y; Grosshans E; de Saint Martin A
Genet Couns; 2002; 13(3):281-7. PubMed ID: 12416635
[TBL] [Abstract][Full Text] [Related]
16. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
Kulharya AS; Lovell CM; Flannery DB
Am J Med Genet; 2002 Dec; 113(4):367-70. PubMed ID: 12457409
[TBL] [Abstract][Full Text] [Related]
17. Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q.
Portnoï MF; Boutchneï S; Bouscarat F; Morlier G; Nizard S; Dersarkissian H; Crickx B; Nouchy M; Taillemite JL; Belaich S
J Med Genet; 1999 Mar; 36(3):246-50. PubMed ID: 10204855
[TBL] [Abstract][Full Text] [Related]
18. A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.
Hu J; Shekhter-Levin S; Shaw PH; Bay C; Kochmar S; Surti U
Cancer Genet Cytogenet; 2005 Jan; 156(1):62-7. PubMed ID: 15588858
[TBL] [Abstract][Full Text] [Related]
19. [Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].
Ronger S; Till M; Kanitakis J; Balme B; Thomas L
Ann Dermatol Venereol; 2003 Nov; 130(11):1033-8. PubMed ID: 14724538
[TBL] [Abstract][Full Text] [Related]
20. Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism.
Magenis E; Webb MJ; Spears B; Opitz JM
Am J Med Genet; 1999 Dec; 87(5):375-83. PubMed ID: 10594874
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
