198 related articles for article (PubMed ID: 12533823)
1. Prenatal management of mosaic tetrasomy 5p.
Reddy KS; Huang B
Prenat Diagn; 2003 Jan; 23(1):82-5. PubMed ID: 12533823
[No Abstract] [Full Text] [Related]
2. Prenatal diagnosis of mosaic tetrasomy 5p.
Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
[TBL] [Abstract][Full Text] [Related]
3. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
[TBL] [Abstract][Full Text] [Related]
4. Diagnosis and clinical delineation of mosaic tetrasomy 5p.
Blakey-Cheung S; Parker P; Schlaff W; Monseur B; Keppler-Noreuil K; Al-Kouatly HB
Eur J Med Genet; 2020 Jan; 63(1):103634. PubMed ID: 30797979
[TBL] [Abstract][Full Text] [Related]
5. Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
Wilson SC; Susman M; Bain S; Wohlferd M; Van Dyke D; Daniel A; White B; Gardner RJ
Prenat Diagn; 2002 Aug; 22(8):681-5. PubMed ID: 12210576
[TBL] [Abstract][Full Text] [Related]
6. Tetrasomy 12p--unusual presentation in CVS.
Dong L; Falk RE; Williams J; Kohan M; Schreck RR
Prenat Diagn; 2003 Feb; 23(2):101-3. PubMed ID: 12575013
[TBL] [Abstract][Full Text] [Related]
7. Tetrasomy 5p mosaicism due to an additional isochromosome 5p in a man with normal phenotype.
Venci A; Bettio D
Am J Med Genet A; 2009 Dec; 149A(12):2889-91. PubMed ID: 19938082
[No Abstract] [Full Text] [Related]
8. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
Polityko AD; Goncharova E; Shamgina L; Drozdovskaja N; Podleschuk L; Abramchik E; Jaroshevich E; Khurs O; Pisarik I; Pribushenya O; Rumyantseva N; Naumchik I
J Histochem Cytochem; 2005 Mar; 53(3):361-4. PubMed ID: 15750020
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis.
Wu YC; Yu MT; Chen LC; Chen CL; Yang ML
Am J Med Genet A; 2003 Mar; 117A(3):278-81. PubMed ID: 12599193
[TBL] [Abstract][Full Text] [Related]
10. Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype.
Goumy C; Beaufrère AM; Francannet C; Tchirkov A; Laurichesse Delmas H; Geissler F; Lemery D; Dechelotte PJ; Vago P
Prenat Diagn; 2005 Aug; 25(8):653-5. PubMed ID: 16049989
[TBL] [Abstract][Full Text] [Related]
11. Mosaic 5p tetrasomy.
Stanley WS; Powell CM; Devine GC; Ellingham T; Samango-Sprouse CA; Vaught DR; Murphy BA; Rosenbaum KN
Am J Med Genet; 1993 Mar; 45(6):774-6. PubMed ID: 8456861
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
Wu YC; Fang JS; Lee KF; Estipona J; Yang ML; Yuan CC
Prenat Diagn; 2003 Feb; 23(2):124-7. PubMed ID: 12575018
[TBL] [Abstract][Full Text] [Related]
13. Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].
Sijmons RH; Leegte B; van Lingen RA; de Pater JM; van der Veen AY; del Canho H; Bos C; ten Kate LP; Breed AS
Am J Med Genet; 1993 Sep; 47(4):559-62. PubMed ID: 7504882
[TBL] [Abstract][Full Text] [Related]
14. Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.
Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
[TBL] [Abstract][Full Text] [Related]
15. Tetrasomy 18p caused by paternal meiotic nondisjunction.
Eggermann T; Engels H; Apacik C; Moskalonek B; Müller-Navia J; Schwanitz G; Stengel-Rutkowski S
Eur J Hum Genet; 1997; 5(3):175-7. PubMed ID: 9272743
[No Abstract] [Full Text] [Related]
16. Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: case report and review of literature.
Brock JA; Dyack S; Ludman M; Dumas N; Gaudet M; Morash B
Am J Med Genet A; 2012 Feb; 158A(2):406-11. PubMed ID: 22247041
[TBL] [Abstract][Full Text] [Related]
17. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
18. Second-trimester diagnosis of mosaic idic(20)(p11) confined to amniocytes without an abnormal phenotype.
Chen CP
Genet Couns; 2003; 14(4):439-41. PubMed ID: 14738121
[No Abstract] [Full Text] [Related]
19. Detection of mosaic isochromosome 20q in amniotic fluid in a pregnancy with fetal arthrogryposis multiplex congenita and normal karyotype in fetal blood and postnatal samples of placenta, skin, and liver.
Chen CP
Prenat Diagn; 2003 Jan; 23(1):85-7. PubMed ID: 12533820
[No Abstract] [Full Text] [Related]
20. Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
Lebbar A; Viot G; Szpiro-Tapia S; Baverel F; Rabineau D; Dupont JM
Prenat Diagn; 2002 Nov; 22(11):973-5. PubMed ID: 12424758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
