In utero first trimester exposure to low‐dose methotrexate with increased fetal nuchal translucency and associated malformations (English)
- New search for: Krähenmann, F.
- New search for: Østensen, M.
- New search for: Stallmach, Th.
- New search for: Huch, A.
- New search for: Chaoui, R.
- New search for: Krähenmann, F.
- New search for: Østensen, M.
- New search for: Stallmach, Th.
- New search for: Huch, A.
- New search for: Chaoui, R.
In:
Prenatal Diagnosis
;
22
, 6
;
489-490
;
2002
- Article (Journal) / Electronic Resource
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Title:In utero first trimester exposure to low‐dose methotrexate with increased fetal nuchal translucency and associated malformations
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Contributors:Krähenmann, F. ( author ) / Østensen, M. ( author ) / Stallmach, Th. ( author ) / Huch, A. ( author ) / Chaoui, R. ( author )
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Published in:Prenatal Diagnosis ; 22, 6 ; 489-490
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Publisher:
- New search for: John Wiley & Sons, Ltd.
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Publication date:2002-06-01
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Size:2 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 22, Issue 6
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 453
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Invasive testing for the karyotyping of mid‐trimester intrauterine fetal death (IUFD): a pilot studyHowarth, E. S. / Konje, J. C. / Healey, K. A. / Duckett, D. P. / Scudamore, I. W. / Taylor, D. J. et al. | 2002
- 456
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Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluidChadefaux‐Vekemans, B. / Rabier, D. / Chabli, A. / Blanc, A. / Aupetit, J. / Bardet, J. / Kamoun, P. et al. | 2002
- 459
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Pilot study for the neonatal screening of fragile X syndromeRifé, M. / Mallolas, J. / Badenas, C. / Tazón, B. / Miguélez, M. Rodríguez / Pàmpols, T. / Sànchez, A. / Milà, M. et al. | 2002
- 463
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Expandability of haemopoietic progenitors in first trimester fetal and maternal blood: implications for non‐invasive prenatal diagnosisCampagnoli, Cesare / Roberts, Irene A. G. / Kumar, Sailesh / Choolani, Mahesh / Bennett, Phillip R. / Letsky, Elizabeth / Fisk, Nicholas M. et al. | 2002
- 470
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Pallister‐Killian syndrome: difficulties of prenatal diagnosisDoray, Bérénice / Girard‐Lemaire, Françoise / Gasser, Bernard / Baldauf, Jean‐Jacques / de Geeter, Bernard / Spizzo, Michèle / Zeidan, Charles / Flori, Elisabeth et al. | 2002
- 478
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The role of hyperglycosylated hCG in trophoblast invasion and the prediction of subsequent pre‐eclampsiaBahado‐Singh, R. O. / Oz, A. U. / Kingston, J. M. / Shahabi, S. / Hsu, C. D. / Cole, L. et al. | 2002
- 482
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An increase in cost‐effectiveness of first trimester maternal screening programmes for fetal chromosome anomalies is obtained by contingent testingChristiansen, Michael / Olesen Larsen, Severin et al. | 2002
- 487
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First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)Martin‐Denavit, T. / Attia‐Sobol, J. / Theuil, J. / Abel‐Lablanche, K. / Boggio, D. / Teyssier, M. / Till, M. / Champion, F. / Vitrey, D. / Plauchu, H. et al. | 2002
- 489
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In utero first trimester exposure to low‐dose methotrexate with increased fetal nuchal translucency and associated malformationsKrähenmann, F. / Østensen, M. / Stallmach, Th. / Huch, A. / Chaoui, R. et al. | 2002
- 490
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Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scanMaymon, R. / Herman, A. / Reish, O. et al. | 2002
- 492
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Trisomy 18 in a fetus with normal NT and abnormal maternal serum biochemistryDe Biasio, Pierangela / Canini, Silvana / Prefumo, Federico / Luigi Venturini, Pier et al. | 2002
- 493
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Mucopolysaccharidosis VII (Sly disease) as a cause of increased nuchal translucency and non‐immune fetal hydrops: study of a family and technical approach to prenatal diagnosis in early and late pregnancyGeipel, A. / Berg, C. / Germer, U. / Krapp, M. / Kohl, M. / Gembruch, U. et al. | 2002
- 495
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Varix of the portal vein: prenatal diagnosis in a fetus with mosaic trisomy 9 syndromeTseng, Jenn‐Jhy / Chou, Min‐Min / Shih‐Chu Ho, Esther et al. | 2002
- 497
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Two more possible pitfalls of rapid prenatal diagnostics using interphase nucleiLiehr, Thomas / Schreyer, Isolde / Neumann, Annett / Beensen, Volkmar / Ziegler, Monika / Hartmann, Isabell / Starke, Heike / Heller, Anita / Nietzel, Angela / Claussen, Uwe et al. | 2002
- 499
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Application of monopolar thermocoagulation in an acardiac fetusChao, An‐Shine / Hsieh, Ching‐Chang / Liou, Jui‐Der / Soong, Yung‐Kuei et al. | 2002
- 503
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Non‐disclosing preimplantation genetic diagnosis for Huntington diseaseStern, Harvey J. / Harton, Gary L. / Sisson, Michael E. / Jones, Shirley L. / Fallon, Lee A. / Thorsell, Lilli P. / Getlinger, Michael E. / Black, Susan H. / Schulman, Joseph D. et al. | 2002
- 508
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Attitude of at‐risk subjects towards preimplantation genetic diagnosis of α‐ and β‐thalassaemias in Hong KongWah Hui, Pui / Lam, Yung Hang / Chen, Min / Tang, Mary Hoi Yin / Yeung, William Shu Biu / Ng, Ernest Hung Yu / Ho, Pak Chung et al. | 2002
- 512
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Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a reviewWilton, Leeanda et al. | 2002
- 519
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First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)Abou‐Sleiman, P. M. / Apessos, A. / Harper, J. C. / Serhal, P. / Winston, R. M. L. / Delhanty, J. D. A. et al. | 2002
- 525
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Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disordersHarper, Joyce C. / Wells, Dagan / Piyamongkol, Wirawit / Abou‐Sleiman, Patrick / Apessos, Angela / Ioulianos, Antonis / Davis, Mary / Doshi, Alpesh / Serhal, Paul / Ranieri, Massimo et al. | 2002
- 534
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Current Awareness| 2002