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Results: 1 to 20 of 143

1.

Three-dimensional ultrasonographic visualization of fetal chromosome abnormalities: a preliminary experience report of 4 cases.

Komwilaisak R, Ratanasiri T, Kleebkaow P.

J Med Assoc Thai. 2004 Oct;87 Suppl 3:S38-44.

PMID:
21213493
[PubMed - indexed for MEDLINE]
2.

Three-dimensional ultrasonographic findings of the rare chromosomal abnormality 48, XXY/+18: a case report.

Komwilaisak R, Ratanasiri T, Komwilaisak P, Luengwattanawanit S.

J Med Assoc Thai. 2004 Feb;87(2):198-203.

PMID:
15061304
[PubMed - indexed for MEDLINE]
3.

Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe.

Stoll C, Garne E, Clementi M; EUROSCAN Study Group.

Prenat Diagn. 2001 Apr;21(4):243-52.

PMID:
11288111
[PubMed - indexed for MEDLINE]
4.

The ultrasound markers of chromosomal disease: a retrospective study.

Twining P, Zuccollo J.

Br J Radiol. 1993 May;66(785):408-14.

PMID:
8319061
[PubMed - indexed for MEDLINE]
5.

Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population.

Stoll C, Dott B, Alembik Y, Roth MP.

Hum Genet. 1993 Mar;91(1):37-41.

PMID:
8454285
[PubMed - indexed for MEDLINE]
6.

Sonographic recognition of major malformations and aberrant fetal growth in trisomic fetuses.

Dicke JM, Crane JP.

J Ultrasound Med. 1991 Aug;10(8):433-8.

PMID:
1834860
[PubMed - indexed for MEDLINE]
Free Article
7.

[Correlation of fetal chromosomal abnormalities to prenatal ultrasound features].

Chen CH, Qiu YW, Chang QX, Yin AL.

Nan Fang Yi Ke Da Xue Xue Bao. 2011 Feb;31(2):347-9. Chinese.

PMID:
21354928
[PubMed - indexed for MEDLINE]
Free Article
8.

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.

Prenat Diagn. 2002 Jan;22(1):29-33.

PMID:
11810646
[PubMed - indexed for MEDLINE]
9.

Double-outlet single ventricle and an abdominal vascular mass: in utero diagnosis with pathological confirmation.

Duncan WJ, George D, Ezzat W, Wallace K, Van den Beuken B.

Pediatr Cardiol. 1993 Jan;14(1):37-9.

PMID:
8456020
[PubMed - indexed for MEDLINE]
10.

[Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].

Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E.

Z Geburtshilfe Neonatol. 1996 Sep-Oct;200(5):186-90. German.

PMID:
9035828
[PubMed - indexed for MEDLINE]
11.

Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population.

Drummond CL, Gomes DM, Senat MV, Audibert F, Dorion A, Ville Y.

Prenat Diagn. 2003 Dec 30;23(13):1068-72.

PMID:
14691994
[PubMed - indexed for MEDLINE]
12.

[Ultrasound screening for Down syndrome and other chromosomal abnormalities by fetal nuchal translucency measurement between 11-14 weeks of gestation].

Dimitrova V, Markov D, Chernev T, Karag'ozova Zh, Mazneĭkova V, Andonova S, Vŭzharova R.

Akush Ginekol (Sofiia). 2005;44(1):32-7. Bulgarian.

PMID:
15853009
[PubMed - indexed for MEDLINE]
13.

Sonographic findings in fetuses with common chromosome abnormalities.

Donnenfeld AE, Mennuti MT.

Clin Obstet Gynecol. 1988 Mar;31(1):80-96. Review.

PMID:
2966025
[PubMed - indexed for MEDLINE]
14.

Ultrasonographically detectable markers of fetal chromosomal abnormalities.

Nicolaides KH, Snijders RJ, Gosden CM, Berry C, Campbell S.

Lancet. 1992 Sep 19;340(8821):704-7.

PMID:
1355807
[PubMed - indexed for MEDLINE]
15.

Contribution of 3D ultrasound and fetal face studies to the prenatal diagnosis of Pallister-Killian syndrome.

Sananes N, Guigue V, Vayssiere C, Kohler M, Girard-Lemaire F, Flori E, Carelle-Calmels N, Boehm N, Samama B, Doray B, Favre R.

J Matern Fetal Neonatal Med. 2010 Jun;23(6):558-62. doi: 10.3109/14767050903214558.

PMID:
19718583
[PubMed - indexed for MEDLINE]
16.

Fetal head-to-trunk volume ratio in chromosomally abnormal fetuses at 11 + 0 to 13 + 6 weeks of gestation.

Falcon O, Cavoretto P, Peralta CF, Csapo B, Nicolaides KH.

Ultrasound Obstet Gynecol. 2005 Dec;26(7):755-60.

PMID:
16163740
[PubMed - indexed for MEDLINE]
Free Article
17.

The use of second-trimester genetic sonogram in guiding clinical management of patients at increased risk for fetal trisomy 21.

Vintzileos AM, Campbell WA, Rodis JF, Guzman ER, Smulian JC, Knuppel RA.

Obstet Gynecol. 1996 Jun;87(6):948-52.

PMID:
8649704
[PubMed - indexed for MEDLINE]
18.

Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe.

De Vigan C, Baena N, Cariati E, Clementi M, Stoll C; EUROSCAN Working Group.

Ann Genet. 2001 Oct-Dec;44(4):209-17.

PMID:
11755107
[PubMed - indexed for MEDLINE]
19.

[Prenatal diagnosis. Review, personal and prospective studies].

Engel E, Empson J, DeLozier D, McGee B, da Costa Woodson E, Engel-de Montmollin M, Carter T, Lorber C, Cassidy SB, Millis J, Heller RM, Boehm F, Vanhooydonk J.

Schweiz Med Wochenschr. 1979 Jul 7;109(27):998-1010. French.

PMID:
88763
[PubMed - indexed for MEDLINE]
20.

Sonographic scoring index for prenatal detection of chromosomal abnormalities.

Benacerraf BR, Neuberg D, Bromley B, Frigoletto FD Jr.

J Ultrasound Med. 1992 Sep;11(9):449-58.

PMID:
1283415
[PubMed - indexed for MEDLINE]
Free Article

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