280 related articles for article (PubMed ID: 12478643)
1. Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report.
Phadke SR; Thakur S
Prenat Diagn; 2002 Dec; 22(13):1240-1. PubMed ID: 12478643
[No Abstract] [Full Text] [Related]
2. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
4. First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents.
Tonni G; Azzoni D; Panteghini M; Ventura A; Cavalli P
Congenit Anom (Kyoto); 2007 Sep; 47(3):101-4. PubMed ID: 17688469
[TBL] [Abstract][Full Text] [Related]
5. Iniencephaly and chromosome mosaicism: a report of two cases.
Halder A; Agarwal S; Pandey A
Congenit Anom (Kyoto); 2005 Sep; 45(3):102-5. PubMed ID: 16131369
[TBL] [Abstract][Full Text] [Related]
6. Double aneuploid mosaicism 45,X/46,XX/47,XX,+18 in a fetus with cerebral malformations.
Picone O; Hirt R; Brisset S; Frydman R; Senat MV; Tachdjian G
Prenat Diagn; 2006 Aug; 26(8):755-7. PubMed ID: 16865741
[No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of a possible new middle interhemispheric variant of holoprosencephaly using sonographic and magnetic resonance imaging.
Picone O; Hirt R; Suarez B; Coulomb A; Tachdjian G; Frydman R; Senat MV
Ultrasound Obstet Gynecol; 2006 Aug; 28(2):229-31. PubMed ID: 16933282
[TBL] [Abstract][Full Text] [Related]
8. Trisomy 22 with holoprosencephaly: a clinicopathologic study.
Isada NB; Bolan JC; Larsen JW; Kent SG
Teratology; 1990 Oct; 42(4):333-6. PubMed ID: 2255998
[TBL] [Abstract][Full Text] [Related]
9. Twin pregnancy discordant for trisomy 14 mosaicism: prenatal sonographic findings.
Sepulveda W; Monckeberg MJ; Be C
Prenat Diagn; 1998 May; 18(5):481-4. PubMed ID: 9621382
[TBL] [Abstract][Full Text] [Related]
10. Prenatal ultrasonographic findings in "trisomy 13".
Pitukkijronnakorn S; Promsonthi P; Panburana P; Rangsiprakarn R; Chittacharoen A
J Med Assoc Thai; 2008 Nov; 91(11):1651-5. PubMed ID: 19127784
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
Chen CP; Chern SR; Hsu CY; Lee CC; Lee MS; Wang W
Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
[No Abstract] [Full Text] [Related]
12. 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]
13. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
Roberts E; Dunlop J; Davis GS; Churchill D; Davison EV
Prenat Diagn; 2003 Jul; 23(7):564-5. PubMed ID: 12868084
[TBL] [Abstract][Full Text] [Related]
14. A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
Von Beust G; Bartels I; Zoll B
Genet Couns; 2003; 14(1):67-74. PubMed ID: 12725591
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?
Karmous-Benailly H; Tabet AC; Thaly A; Dupuy O; Huten Y; Luton D; Baumann C; Delezoide AL
Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668
[TBL] [Abstract][Full Text] [Related]
16. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
Donaghue C; Mann K; Docherty Z; Ogilvie CM
Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child.
Staals JE; Schrander-Stumpel CT; Hamers G; Fryns JP
Genet Couns; 2003; 14(2):233-7. PubMed ID: 12872819
[TBL] [Abstract][Full Text] [Related]
18. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
[TBL] [Abstract][Full Text] [Related]
19. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
Corsello G; Buttitta P; Cammarata M; Lo Presti A; Maresi E; Zumpani L; Giuffrè L
Am J Med Genet; 1990 Oct; 37(2):244-9. PubMed ID: 2147361
[TBL] [Abstract][Full Text] [Related]
20. Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly.
de Pater JM; Scheres JM; Brons J
Prenat Diagn; 1997 Sep; 17(9):887-8. PubMed ID: 9316141
[No Abstract] [Full Text] [Related]
[Next] [New Search]