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Items: 1 to 20 of 88

1.

Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies.

Roos A, von Kaisenberg CS, Eggermann T, Schwanitz G, Löffler C, Weise A, Mrasek K, Junge A, Caliebe A, Belitz B, Kautza M, Schüler H, Zerres K, Heidemann S.

Arch Gynecol Obstet. 2013 Nov;288(5):1153-8. doi: 10.1007/s00404-013-2861-5. Epub 2013 May 16.

PMID:
23677416
2.

Mutations of the SYCP3 gene in women with recurrent pregnancy loss.

Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H.

Am J Hum Genet. 2009 Jan;84(1):14-20. doi: 10.1016/j.ajhg.2008.12.002. Epub 2008 Dec 24.

3.

SYCP3 mutation may not be associated with recurrent miscarriage caused by aneuploidy.

Mizutani E, Suzumori N, Ozaki Y, Oseto K, Yamada-Namikawa C, Nakanishi M, Sugiura-Ogasawara M.

Hum Reprod. 2011 May;26(5):1259-66. doi: 10.1093/humrep/der035. Epub 2011 Feb 26.

PMID:
21357605
4.

Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage.

Hanna CW, Blair JD, Stephenson MD, Robinson WP.

Reprod Biomed Online. 2012 Feb;24(2):251-3. doi: 10.1016/j.rbmo.2011.10.013. Epub 2011 Nov 3.

PMID:
22197129
5.

Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population.

Gurkan H, Aydin F, Kadıoglu A, Palanduz S.

Andrologia. 2013 Apr;45(2):92-100. doi: 10.1111/j.1439-0272.2012.01317.x. Epub 2012 Jun 6.

PMID:
22670862
6.

[Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].

Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.

Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):644-8. Chinese.

PMID:
22176986
7.

The association between sporadic somatic parental aneuploidy and chromosomally abnormal placentae in habitual abortions.

Daniely M, Aviram A, Carp HJ, Shaki R, Barkai G.

Early Pregnancy. 2001 Jul;5(3):153-63.

PMID:
11753529
8.

Cell-free fetal DNA in amniotic fluid: unique fragmentation signatures in euploid and aneuploid fetuses.

Lapaire O, Bianchi DW, Peter I, O'Brien B, Stroh H, Cowan JM, Tantravahi U, Johnson KL.

Clin Chem. 2007 Mar;53(3):405-11. Epub 2007 Jan 26.

9.

Genetic factors as a cause of miscarriage.

Suzumori N, Sugiura-Ogasawara M.

Curr Med Chem. 2010;17(29):3431-7. Review.

PMID:
20712563
10.

The T657C polymorphism on the SYCP3 gene is associated with recurrent pregnancy loss.

Sazegari A, Kalantar SM, Pashaiefar H, Mohtaram S, Honarvar N, Feizollahi Z, Ghasemi N.

J Assist Reprod Genet. 2014 Oct;31(10):1377-81. doi: 10.1007/s10815-014-0272-6. Epub 2014 Jul 25.

11.
12.

Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR.

Bili C, Divane A, Apessos A, Konstantinos T, Apostolos A, Ioannis B, Periklis T, Florentin L.

Prenat Diagn. 2002 May;22(5):360-5.

PMID:
12001187
13.

Azoospermia in patients heterozygous for a mutation in SYCP3.

Miyamoto T, Hasuike S, Yogev L, Maduro MR, Ishikawa M, Westphal H, Lamb DJ.

Lancet. 2003 Nov 22;362(9397):1714-9.

PMID:
14643120
14.
15.

Chromosome analysis of aborted conceptuses of recurrent aborters positive for anticardiolipin antibody.

Takakuwa K, Asano K, Arakawa M, Yasuda M, Hasegawa I, Tanaka K.

Fertil Steril. 1997 Jul;68(1):54-8.

PMID:
9207584
16.

Mutation screening of AURKB and SYCP3 in patients with reproductive problems.

López-Carrasco A, Oltra S, Monfort S, Mayo S, Roselló M, Martínez F, Orellana C.

Mol Hum Reprod. 2013 Feb;19(2):102-8. doi: 10.1093/molehr/gas047. Epub 2012 Oct 25.

PMID:
23100464
17.

Recurrent aneuploidy--fact or fiction.

Cohen R, Check JH.

Clin Exp Obstet Gynecol. 2010;37(3):175-7.

PMID:
21077516
18.

Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype.

Hassold T, Jacobs PA, Pettay D.

Genet Epidemiol. 1988;5(2):65-74.

PMID:
3402725
19.

Karyotype of the abortus in recurrent miscarriage.

Carp H, Toder V, Aviram A, Daniely M, Mashiach S, Barkai G.

Fertil Steril. 2001 Apr;75(4):678-82.

PMID:
11287018
20.

[Molecular biology usefulness for rapid diagnosis of Down's syndrome and common aneuploidies].

Fauret AL, Bilan F, Patri S, Couet D, Marechaud M, Pierre F, Gilbert-Dussardier B, Kitzis A.

Gynecol Obstet Fertil. 2009 Jul-Aug;37(7-8):611-9. doi: 10.1016/j.gyobfe.2009.05.007. Epub 2009 Jul 1. French.

PMID:
19574080

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