138 related articles for article (PubMed ID: 16575887)
1. Aplasia and duplication of the thumb and facial clefts associated with fetal trisomy 18.
Chen CP
Am J Med Genet A; 2006 May; 140(9):960-3. PubMed ID: 16575887
[No Abstract] [Full Text] [Related]
2. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Chen CP; Chern SR; Chen CY; Wu PC; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):479-84. PubMed ID: 22212321
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
[TBL] [Abstract][Full Text] [Related]
4. Chromosomal defects and associated malformations in fetal cleft lip with or without cleft palate.
Perrotin F; de Poncheville LM; Marret H; Paillet C; Lansac J; Body G
Eur J Obstet Gynecol Reprod Biol; 2001 Nov; 99(1):19-24. PubMed ID: 11604181
[TBL] [Abstract][Full Text] [Related]
5. [Problems posed by the diagnosis and prenatal management of facial clefts].
Perrotin F; Lardy H; Marret H; Paillet C; Lansac J; Body G
Rev Stomatol Chir Maxillofac; 2001 Jun; 102(3-4):143-52. PubMed ID: 11577466
[TBL] [Abstract][Full Text] [Related]
6. Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses.
Bergé SJ; Plath H; Van de Vondel PT; Appel T; Niederhagen B; Von Lindern JJ; Reich RH; Hansmann M
Ultrasound Obstet Gynecol; 2001 Nov; 18(5):422-31. PubMed ID: 11844159
[TBL] [Abstract][Full Text] [Related]
7. A case of Yunis-Varon syndrome complicated with complete cleft lip and palate.
Sumi M; Kusumoto T; Kondoh T; Moriuchi H; Miyamoto M; Masuzaki H; Ishimaru T
Am J Med Genet A; 2004 Feb; 125A(1):92-3. PubMed ID: 14755473
[No Abstract] [Full Text] [Related]
8. Another case of Varadi-Papp Syndrome with a molar tooth sign.
Chodirker BN; Shah NS; Bunge MK; Reed MH
Am J Med Genet A; 2005 Aug; 136A(4):416-7. PubMed ID: 15988746
[No Abstract] [Full Text] [Related]
9. [A case of Patau syndrome. Fetal heart defect and lip-jaw-palate cleft as indicators].
Küffer E; Asseryanis E; Eppel W; Schurz B; Reinold E
Ultraschall Med; 1994 Aug; 15(4):217-8. PubMed ID: 7973594
[TBL] [Abstract][Full Text] [Related]
10. Twin pregnancy with Roberts syndrome in one fetus and trisomy 18 in the other.
Dalal AB; Phadke SR
J Clin Ultrasound; 2006; 34(3):146-9. PubMed ID: 16547991
[TBL] [Abstract][Full Text] [Related]
11. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years].
Chuchracki M; Janiak J; Ziółkowska K; Sedziak A; Opala T
Przegl Lek; 2012; 69(10):1007-10. PubMed ID: 23421080
[TBL] [Abstract][Full Text] [Related]
12. Complexity of noninvasive prenatal screening and diagnostic testing for an unbalanced translocation involving chromosomes 5 and 18.
Feenstra H; Dunn T; Lewis D; Herrera K; Foroutan J; Calabio R; Batey A; Wang E; Gebbia JA
Prenat Diagn; 2014 Feb; 34(2):195-8. PubMed ID: 24214723
[No Abstract] [Full Text] [Related]
13. 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]
14. Fluorescence in situ hybridisation on formalin fixed fetal tissue in the diagnosis of chromosomal syndromes.
Cobben JM; Essed CE; Hirdes J; Kraayenbrink RA; Van der Veen A
Genet Couns; 1994; 5(2):141-5. PubMed ID: 7917121
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 18: first-trimester nuchal translucency with pathological correlation.
Jackson S; Porter H; Vyas S
Ultrasound Obstet Gynecol; 1995 Jan; 5(1):55-6. PubMed ID: 7850592
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis and management of fetal facial clefts.
Saltzman DH; Benacerraf BR; Frigoletto FD
Am J Obstet Gynecol; 1986 Aug; 155(2):377-9. PubMed ID: 3526897
[TBL] [Abstract][Full Text] [Related]
17. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma.
Chen CP; Ko TM; Huang MC; Chern SR; Lin TW; Chang TY; Kuo YL; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2015 Feb; 54(1):78-80. PubMed ID: 25675926
[No Abstract] [Full Text] [Related]
18. Survival with trisomy 18--data from Switzerland.
Niedrist D; Riegel M; Achermann J; Schinzel A
Am J Med Genet A; 2006 May; 140(9):952-9. PubMed ID: 16528741
[TBL] [Abstract][Full Text] [Related]
19. Prenatal detection of D trisomy.
Laurence KM; Gregory PJ; Sharp F
J Med Genet; 1974 Dec; 11(4):398-400. PubMed ID: 4443990
[TBL] [Abstract][Full Text] [Related]
20. Microscopic study of holoprosencephalic facial anomalies in trisomy 13 fetuses.
Sperber GH; Honoré LH; Machin GA
Am J Med Genet; 1989 Apr; 32(4):443-51. PubMed ID: 2773983
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]