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Items: 1 to 20 of 83

1.

Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.

Chen CP, Chen M, Ma GC, Chang SP, Chen YY, Wu PC, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2011 Jun;50(2):253-7. doi: 10.1016/j.tjog.2011.04.007. No abstract available.

2.

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.

Bruyère H, Speevak MD, Winsor EJ, de Fréminville B, Farrell SA, McGowan-Jordan J, McGillivray B, Chitayat D, McFadden D, Adouard V, Terespolsky D, Prieur F, Pantzar T, Hrynchak M.

Prenat Diagn. 2006 Apr;26(4):324-9. Review.

PMID:
16521154
3.

Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations.

Huang B, Thangavelu M, Bhatt S, J Sandlin C, Wang S.

Prenat Diagn. 2002 Feb;22(2):105-10.

PMID:
11857613
4.
5.

Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism.

Eiben B, Unger M, Stoltenberg G, Rutt G, Goebel R, Meyer A, Gamerdinger U, Hammans W, Hansen S, Hauss H, et al.

Prenat Diagn. 1992 Nov;12(11):945-50.

PMID:
1494547
6.

Dandy-Walker malformation in a male fetus with mosaic 45,X/46,X,del(Y)(q11).

Witters I, Vandecruys H, Devlieger R, Fryns JP.

Genet Couns. 2008;19(4):439-41. No abstract available.

PMID:
19239090
7.

[The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome].

Barros BA, Maciel-Guerra AT, De Mello MP, Coeli FB, Carvalho AB, Viguetti-Campos N, Assumpção Jde G, Marques-de-Faria AP, Lemos-Marini SH, Guerra-Junior G.

Arq Bras Endocrinol Metabol. 2009 Dec;53(9):1137-42. Portuguese.

8.

Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.

Hwa HL, Ko TM, Chang YY, Huang CH, Su YN, Tseng LH, Hsieh FJ.

Prenat Diagn. 2004 Feb;24(2):121-4.

PMID:
14974120
9.

Cytogenetic analysis of early nonviable pregnancies after assisted reproduction treatment.

Martínez MC, Méndez C, Ferro J, Nicolás M, Serra V, Landeras J.

Fertil Steril. 2010 Jan;93(1):289-92. doi: 10.1016/j.fertnstert.2009.07.989. Epub 2009 Sep 11.

PMID:
19748088
10.

Prenatal diagnosis of familial ring 21 chromosome.

Melnyk AR, Ahmed I, Taylor JC.

Prenat Diagn. 1995 Mar;15(3):269-73.

PMID:
7784385
11.

Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.

Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen LF, Hua HM, Wang W.

Prenat Diagn. 2006 Apr;26(4):387-91. No abstract available.

PMID:
16566039
13.

Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patients.

Wiktor AE, Van Dyke DL.

Am J Med Genet A. 2005 Oct 15;138A(3):259-61.

PMID:
16158437
14.

Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.

Chien SC, Chen CP, Lin CC, Huang LC, Hsieh CT, Tsai FJ.

Taiwan J Obstet Gynecol. 2009 Sep;48(3):292-5. doi: 10.1016/S1028-4559(09)60307-7. Review.

15.

Molecular cytogenetic analysis of a ring-Y infertile male patient.

Carvalho FM, Wolfgramm EV, Degasperi I, Verbeno BM, Vianna BA, Chagas FF, Perroni AM, Paula F, Louro ID.

Genet Mol Res. 2007 Mar 9;6(1):59-66.

16.

Mix gonadal dysgenesis associated with ring Y chromosome mosaics in a phenotypic male.

Lopez-Valdes JA, Nieto K, Najera N, Cervantes A, Kofman-Alfaro S, Queipo G.

Sex Dev. 2009;3(4):177-82. doi: 10.1159/000228717. Epub 2009 Sep 11.

PMID:
19752596
17.

Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.

Fischer W, Dermitzel A, Osmers R, Pruggmayer M.

Prenat Diagn. 2001 Jun;21(6):481-3.

PMID:
11438954
18.

Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.

de Pater J, Van der Sijs-Bos C, Prins M, Derks J, Albrechts J, Engelen J.

Eur J Med Genet. 2006 Jul-Aug;49(4):306-12. Epub 2006 Jan 19.

PMID:
16461028
19.

Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.

Lebbar A, Viot G, Szpiro-Tapia S, Baverel F, Rabineau D, Dupont JM.

Prenat Diagn. 2002 Nov;22(11):973-5.

PMID:
12424758
20.

Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.

Witters I, Moerman P, Louwagie D, Van Assche FA, Migeon BR, Fryns JP.

Ann Genet. 2001 Oct-Dec;44(4):179-82.

PMID:
11755101

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