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Best matches for The Clinical Indications and Cytogenetic Analysis of Genetic Amniocentesis Cases:

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Items: 15

1.

A retrospective exploratory study of fetal genetic invasive procedures at a University Hospital.

Andrew C, Koshy T, Gopal S, Paul SFD.

J Obstet Gynaecol. 2018 Oct;38(7):906-910. doi: 10.1080/01443615.2018.1433645. Epub 2018 Mar 19.

PMID:
29553859
2.

Retrospective analysis of 4761 cases who underwent amniocentesis in southeast China.

Tao H, Xiao J, Yang C, Wang J, Tang Y, Guo C, Wang J.

J Obstet Gynaecol. 2018 Jan;38(1):38-41. doi: 10.1080/01443615.2017.1326887. Epub 2017 Aug 1.

PMID:
28764586
3.

Clinical and cytogenetic results of a series of amniocentesis cases from Northeast China: a report of 2500 cases.

An N, Li LL, Wang RX, Li LL, Yue JM, Liu RZ.

Genet Mol Res. 2015 Dec 2;14(4):15660-7. doi: 10.4238/2015.December.1.18.

4.

[FREQUENCIES OF FETAL CHROMOSOMAL ABERRATIONS DETECTED BY AMNIOCENTESIS: OUR 15-YEARS EXPERIENCE].

Stoyanova V, Ivanov H, Linev A, Vachev T.

Akush Ginekol (Sofiia). 2015;54(5):13-8. Bulgarian.

PMID:
26411190
5.

[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. Polish.

PMID:
23421080
6.

A prevalent Y;15 translocation in the Ethiopian Beta Israel community in Israel.

Chen-Shtoyerman R, Josefsberg Ben-Yehoshua S, Nissani R, Rosensaft J, Appelman Z.

Cytogenet Genome Res. 2012;136(3):171-4. doi: 10.1159/000336201. Epub 2012 Feb 11.

PMID:
22327880
7.

Evaluation of clinical and cytogenetic findings on 1,068 second-trimester amniocenteses in Southeast Turkey.

Balkan M, Akbas H, Kalkanli S, Sakar MN, Fidanboy M, Alp MN, Budak T.

Clin Exp Obstet Gynecol. 2011;38(4):364-8.

PMID:
22268276
8.

Rapid aneuploidy testing versus traditional karyotyping in amniocentesis for certain referral indications.

Comas C, Echevarria M, Carrera M, Serra B.

J Matern Fetal Neonatal Med. 2010 Sep;23(9):949-55. doi: 10.3109/14767050903334893.

PMID:
20718579
9.

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.

Van den Veyver IB, Patel A, Shaw CA, Pursley AN, Kang SH, Simovich MJ, Ward PA, Darilek S, Johnson A, Neill SE, Bi W, White LD, Eng CM, Lupski JR, Cheung SW, Beaudet AL.

Prenat Diagn. 2009 Jan;29(1):29-39. doi: 10.1002/pd.2127.

10.

Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.

Van Opstal D, Boter M, de Jong D, van den Berg C, Brüggenwirth HT, Wildschut HI, de Klein A, Galjaard RJ.

Eur J Hum Genet. 2009 Jan;17(1):112-21. doi: 10.1038/ejhg.2008.161. Epub 2008 Sep 10.

11.

Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative study.

Karaoguz MY, Bal F, Yakut T, Ercelen NO, Ergun MA, Gokcen AB, Biri AA, Kimya Y, Urman B, Gultomruk M, Egeli U, Menevse S.

Genet Couns. 2006;17(2):219-30.

PMID:
16970041
12.

Isolated polydactyly: prenatal diagnosis and perinatal outcome.

Bromley B, Shipp TD, Benacerraf B.

Prenat Diagn. 2000 Nov;20(11):905-8.

PMID:
11113893
13.

[Clinical approach to prenatal diagnosis of chromosome abnormalities].

Herlicoviez M.

Reprod Nutr Dev. 1990;Suppl 1:139s-145s. Review. French.

PMID:
2206291
15.

Pre-natal counselling and diagnosis in Down's syndrome.

Papp Z.

Med Gynaecol Androl Sociol. 1973;7(4):10-5.

PMID:
12156379

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