99 related articles for article (PubMed ID: 15824490)
1. Prenatal diagnosis, phenotypic and obstetric characteristics of holoprosencephaly.
Joó GJ; Beke A; Papp C; Tóth-Pál E; Szigeti Z; Bán Z; Papp Z
Fetal Diagn Ther; 2005; 20(3):161-6. PubMed ID: 15824490
[TBL] [Abstract][Full Text] [Related]
2. [Hereditary holoprosencephaly--late diagnosis in spite of recurrence].
Geka F; Reitter A; Louwen F
Z Geburtshilfe Neonatol; 2012 Feb; 216(1):37-9. PubMed ID: 22331527
[TBL] [Abstract][Full Text] [Related]
3. The risk of recurrence of holoprosencephaly in euploid fetuses.
David AL; Gowda V; Turnbull C; Chitty LS
Obstet Gynecol; 2007 Sep; 110(3):658-62. PubMed ID: 17766614
[TBL] [Abstract][Full Text] [Related]
4. Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).
Mercier S; Dubourg C; Belleguic M; Pasquier L; Loget P; Lucas J; Bendavid C; Odent S
Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):191-6. PubMed ID: 20104616
[TBL] [Abstract][Full Text] [Related]
5. Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.
Cohen MM; Sulik KK
J Craniofac Genet Dev Biol; 1992; 12(4):196-244. PubMed ID: 1494025
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations.
Goetzinger KR; Stamilio DM; Dicke JM; Macones GA; Odibo AO
Am J Obstet Gynecol; 2008 Sep; 199(3):285.e1-6. PubMed ID: 18771985
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of alobar holoprosencephaly at 10 weeks of gestation.
Turner CD; Silva S; Jeanty P
Ultrasound Obstet Gynecol; 1999 May; 13(5):360-2. PubMed ID: 10380303
[TBL] [Abstract][Full Text] [Related]
11. Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly.
Chen CP; Shih JC; Hsu CY; Chen CY; Huang JK; Wang W
J Clin Ultrasound; 2005; 33(6):312-8. PubMed ID: 16134165
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of holoprosencephaly by transvaginal ultrasonography in the first trimester.
Hamada H; Oki A; Tsunoda H; Kubo T
Asia Oceania J Obstet Gynaecol; 1992 Jun; 18(2):125-9. PubMed ID: 1503536
[TBL] [Abstract][Full Text] [Related]
13. [Prenatal diagnosis of central nervous system malformations].
Langmár Z; Németh M; Csaba Á; Szigeti Z; Joó JG
Ideggyogy Sz; 2013 Jul; 66(7-8):228-34. PubMed ID: 23971353
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations.
Chuang L; Kuo PL; Yang HB; Chien CH; Chen PY; Chang CH; Chang FM
Prenat Diagn; 2003 Feb; 23(2):134-7. PubMed ID: 12575020
[TBL] [Abstract][Full Text] [Related]
15. Fetal holoprosencephaly: associated malformations and chromosomal defects.
Berry SM; Gosden C; Snijders RJ; Nicolaides KH
Fetal Diagn Ther; 1990; 5(2):92-9. PubMed ID: 2130835
[TBL] [Abstract][Full Text] [Related]
16. Risk of recurrence in major central nervous system malformations between 1976 and 2005.
Joó JG; Beke A; Papp Z; Csaba A; Rab A; Papp C
Prenat Diagn; 2007 Nov; 27(11):1028-32. PubMed ID: 17694579
[TBL] [Abstract][Full Text] [Related]
17. Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil.
Richieri-Costa A; Ribeiro LA
Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):149-57. PubMed ID: 20104612
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Skewed sex ratios in familial holoprosencephaly and in people with isolated single maxillary central incisor.
Suthers G; Smith S; Springbett S
J Med Genet; 1999 Dec; 36(12):924-6. PubMed ID: 10594002
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]