228 related articles for article (PubMed ID: 16302165)
21. First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).
Martin-Denavit T; Attia-Sobol J; Theuil J; Abel-Lablanche K; Boggio D; Teyssier M; Till M; Champion F; Vitrey D; Plauchu H
Prenat Diagn; 2002 Jun; 22(6):487-9. PubMed ID: 12116308
[No Abstract] [Full Text] [Related]
22. False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism.
Gao Y; Stejskal D; Jiang F; Wang W
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):477-8. PubMed ID: 24186002
[No Abstract] [Full Text] [Related]
23. A live-born child with a mosaic chromosomal pattern of either monosomy 21 or trisomy 4 in different embryonal germ layers.
van der Kevie-Kersemaekers AM; Suijkerbuijk RF; Moll FC; Dijkhuizen T; van Spaendonck-Zwarts KY; Drok G; Bouman K; Sikkema-Raddatz B
Prenat Diagn; 2010 Jan; 30(1):86-8. PubMed ID: 19960447
[No Abstract] [Full Text] [Related]
24. Prenatal diagnosis of mosaic trisomy 9.
Chen CP; Hung FY; Su YN; Chern SR; Su JW; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):549-53. PubMed ID: 22212338
[No Abstract] [Full Text] [Related]
25. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
Chen CP; Lin CC; Chang TY; Li YC; Hsieh LJ; Lee CC; Chen LF; Wang W
Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
[No Abstract] [Full Text] [Related]
26. Prenatal diagnosis of sub-microscopic partial trisomy 10q using chromosomal microarray analysis in a phenotypically abnormal fetus with normal karyotype.
Browne PC; Adam S; Badr M; Brooks CR; Edwards J; Walker P; Mohamed S; Gregg AR
J Neonatal Perinatal Med; 2016 May; 9(2):217-22. PubMed ID: 27197934
[TBL] [Abstract][Full Text] [Related]
27. Fetal t(5p;21q) misdiagnosed as monosomy 21: a plea for in situ hybridization studies.
Gill P; Uhrich S; Disteche C; Cheng E
Am J Med Genet; 1994 Oct; 52(4):416-8. PubMed ID: 7747753
[TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis of a partial 6q trisomy: a case report.
Valerio D; Di Domenico A; Felicetti M; La Boccetta A; Ferrara C; Antonio N; Borrelli AL
Prenat Diagn; 2006 Oct; 26(10):917-9. PubMed ID: 16845680
[TBL] [Abstract][Full Text] [Related]
29. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
Bregant L; Gersak K; Veble A
Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.
Hu H; Hao J; Yao H; Chang Q; Li R; Zhang X; Liang Z
Gene; 2013 Mar; 517(1):132-6. PubMed ID: 23232358
[TBL] [Abstract][Full Text] [Related]
31. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations.
Chen CP; Chern SR; Tsai EJ; Lee CC; Chen LF; Wang W
Genet Couns; 2009; 20(3):281-8. PubMed ID: 19852436
[No Abstract] [Full Text] [Related]
32. Natural history of fetal trisomy 18 after prenatal diagnosis.
Burke AL; Field K; Morrison JJ
Arch Dis Child Fetal Neonatal Ed; 2013 Mar; 98(2):F152-4. PubMed ID: 22562870
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
Chen CP; Chang YL; Chern SR; Wu PS; Su JW; Chen WL; Chen LF; Wang W
Gene; 2013 Mar; 516(1):132-7. PubMed ID: 23266805
[TBL] [Abstract][Full Text] [Related]
34. Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
Bornstein E; Barnhard Y; Donnenfeld A; Ferber A; Divon MY
Obstet Gynecol; 2006 Apr; 107(4):877-9. PubMed ID: 16582126
[TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis in human immunodeficiency virus-infected women: a new screening program for chromosomal anomalies.
Coll O; Suy A; Hernandez S; Pisa S; Lonca M; Thorne C; Borrell A
Am J Obstet Gynecol; 2006 Jan; 194(1):192-8. PubMed ID: 16389031
[TBL] [Abstract][Full Text] [Related]
36. [A case of 18-trisomy diagnosed by fluorescence in situ hybridization of amniocyte].
Maruyama H; Fukushi Y; Tando T; Wada J; Niino T; Sato S; Kagiya A; Sato S; Saito Y
Nihon Sanka Fujinka Gakkai Zasshi; 1994 Jul; 46(7):611-3. PubMed ID: 8089600
[No Abstract] [Full Text] [Related]
37. Positive biochemical screening for trisomy 18: on the path of trisomy 9.
Póvoa A; Ramalho C; Torgal A; Brandão O; Matias A; Oliveira MJ; Montenegro N; Castedo S
Prenat Diagn; 2008 Feb; 28(2):162-4. PubMed ID: 18236431
[No Abstract] [Full Text] [Related]
38. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
[TBL] [Abstract][Full Text] [Related]
39. Prenatally diagnosed trisomy 6 mosaicism.
Gupta N; Pradhan M; Manisha ; Singh R; Phadke SR
Prenat Diagn; 2004 Oct; 24(10):841-4. PubMed ID: 15503282
[No Abstract] [Full Text] [Related]
40. Prenatally detected trisomy 20 mosaicism.
Robinson WP; McGillivray B; Lewis ME; Arbour L; Barrett I; Kalousek DK
Prenat Diagn; 2005 Mar; 25(3):239-44. PubMed ID: 15791659
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]