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Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W.
Taiwan J Obstet Gynecol. 2011 Dec;50(4):506-11
22212326
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A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP, Huang HK, Ling PY, Su YN, Chen M, Tsai FJ, Wu PC, Chern SR, Chen YT, Lee CC, Wang W.
Taiwan J Obstet Gynecol. 2011 Dec;50(4):492-8
22212323
[PubMed - in process] nohighlight
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Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP, Su YN, Hsu CY, Chern SR, Lee CC, Chen YT, Chen WL, Wang W.
Taiwan J Obstet Gynecol. 2011 Dec;50(4):485-91
22212322
[PubMed - in process] nohighlight
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Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Chen CP, Chern SR, Chen CY, Wu PC, Chen LF, Pan CW, Wang W.
Taiwan J Obstet Gynecol. 2011 Dec;50(4):479-84
22212321
[PubMed - in process] nohighlight
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Prenatal diagnosis: types and techniques.
Collins SL, Impey L.
Early Hum Dev. 2012 Jan;88(1):3-8. doi: 10.1016/j.earlhumdev.2011.11.003. Review
22196141
[PubMed - indexed for MEDLINE] nohighlight
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[The role of infection in preterm birth].
Petit E, Abergel A, Dedet B, Subtil D.
J Gynecol Obstet Biol Reprod (Paris). 2012 Feb;41(1):14-25. Epub 2011 Dec 20. Review. French.
22192232
[PubMed - indexed for MEDLINE] nohighlight
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Amniocentesis performed for karyotyping after identified ultrasonographic abnormalities: what to expect?
Gaudry P, Esvan M, Meynard JB, Lebbar A, Choiset A, Lewin F, Tsatsaris V, Pannier E, Grange G.
Fetal Diagn Ther. 2012;31(1):55-62. Epub 2011 Dec 13
22189057
[PubMed - in process] nohighlight
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Prenatally diagnosed 17q12 microdeletion syndrome with a novel association with congenital diaphragmatic hernia.
Hendrix NW, Clemens M, Canavan TP, Surti U, Rajkovic A.
Fetal Diagn Ther. 2012;31(2):129-33. Epub 2011 Dec 14
22178801
[PubMed - in process] nohighlight
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[Study on key techniques and intervention in reducing birth defects].
Zhu BS, Su J, Lu XH, He J, Zhu S, Jiao CX, Zhang JM, Tang XH, Tao Y, Lin KP, Chen H, Li SY.
Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):658-63. Chinese.
22176989
[PubMed - in process] nohighlight
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[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.
22176986
[PubMed - in process] nohighlight
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Prenatal diagnosis of xeroderma pigmentosum group A in Japan.
Moriwaki S, Yamashita Y, Nakamura S, Fujita D, Kohyama J, Takigawa M, Ohmichi M.
J Dermatol. 2012 Jun;39(6):516-9. doi: 10.1111/j.1346-8138.2011.01425.x. Epub 2011 Dec 14
22168765
[PubMed - in process] nohighlight
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Intra-amniotic sludge in a woman with asymptomatic cervical dilatation.
Rhalmi N, Himaya E, Girard M, Bujold E.
J Obstet Gynaecol Can. 2011 Dec;33(12):1201. No abstract available.
22166271
[PubMed - indexed for MEDLINE] nohighlight
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Fetal Anterior Wall Thickness and Amniotic Fluid Insulin Levels: an Interdependence?
Ulrich D, Desoye G, Wadsack C, Haas J, Csapo B, Holzapfel-Bauer M, Lang U, Schlembach D.
Ultraschall Med. 2011 Dec 9. [Epub ahead of print
22161616
[PubMed - as supplied by publisher] nohighlight
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[Synpolydactyly in a Chinese kindred: mutation detection, prenatal ultrasonographic and molecular diagnosis].
Jin H, Lin PF, Wang QM, Mao F, Cai Y, Gong YQ.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):601-5. Chinese.
22161087
[PubMed - indexed for MEDLINE] nohighlight
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Gene expression analysis of amniotic fluid: new biomarkers and novel antenatal treatments.
Bianchi DW.
Clin Biochem. 2011 May;44(7):448-50. No abstract available.
22145168
[PubMed - indexed for MEDLINE] nohighlight
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An atypical strain associated with congenital toxoplasmosis in Tunisia.
Boughattas S, Abdallah RB, Siala E, Aoun K, Bouratbine A.
New Microbiol. 2011 Oct;34(4):413-6. Epub 2011 Oct 31
22143816
[PubMed - indexed for MEDLINE] Free Article nohighlight
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Pregnancy Loss after Chorionic Villus Sampling and Genetic Amniocentesis in Twin Pregnancies- a Systematic Review.
Agarwal K, Alfirevic Z.
Ultrasound Obstet Gynecol. 2011 Nov 28. doi: 10.1002/uog.10152. [Epub ahead of print
22125091
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Umbilical cord hernias: prenatal diagnosis and natural history.
Haas J, Achiron R, Barzilay E, Yinon Y, Bilik R, Gilboa Y.
J Ultrasound Med. 2011 Dec;30(12):1629-32
22123997
[PubMed - indexed for MEDLINE] nohighlight
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Antibiotic prophylaxis before amniocentesis.
Hobbins JC, Pilu G, Abuhumad A, Alfirevic Z, Bahado-Singh RO, Benacerraf BR, Berkowitz RL, Cetin I, Copel JA, Eik-Nes S, Frusca T, Galan HL, Guaschino S, Mahoney MJ, Marsal K, Malinger G, Marconi AM, Martinelli P, Moore TR, Papageorghiou AT, Platt LD, Rizzo N, Tabor A, Thilaganathan B, Timor-Tritsch IE, Todros T, Yagel S.
Prenat Diagn. 2011 Dec;31(12):1213-4; author reply 1215. doi: 10.1002/pd.2842. No abstract available.
22120439
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The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
Claes K, Dahan K, Tejpar S, De Paepe A, Bonduelle M, Abramowicz M, Verellen C, Franchimont D, Van Cutsem E, Kartheuser A.
Acta Gastroenterol Belg. 2011 Sep;74(3):421-6. Review
22103048
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