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Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo).
Bettelheim D, Hengstschläger M, Drahonsky R, Eppel W, Bernaschek G. Bettelheim D, et al. Among authors: bernaschek g. Clin Genet. 1998 Apr;53(4):319-20. doi: 10.1111/j.1399-0004.1998.tb02706.x. Clin Genet. 1998. PMID: 9650775 No abstract available.
Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature.
Hengstschläger M, Mittermayer C, Repa C, Drahonsky R, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: bernaschek g. Fetal Diagn Ther. 2004 Nov-Dec;19(6):510-2. doi: 10.1159/000080164. Fetal Diagn Ther. 2004. PMID: 15539876 Review.
Raising the sensitivity of fetal RhD typing and sex determination from maternal blood.
Hengstschläger M, Hölzl G, Ulm B, Bernaschek G. Hengstschläger M, et al. Among authors: bernaschek g. J Med Genet. 1997 Apr;34(4):350-1. doi: 10.1136/jmg.34.4.350-b. J Med Genet. 1997. PMID: 9138165 Free PMC article. No abstract available.
Prenatal diagnosis of a de novo inversion of chromosome (2)(p21q11).
Hengstschläger M, Mittermayer C, Prusa AR, Drahonsky R, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: bernaschek g. Arch Gynecol Obstet. 2003 Aug;268(3):230-2. doi: 10.1007/s00404-002-0313-8. Epub 2002 May 15. Arch Gynecol Obstet. 2003. PMID: 12942256 Review.
The clinical impact of magnetic resonance imaging in fetuses with central nervous system anomalies on ultrasound scan.
Blaicher W, Prayer D, Mittermayer C, Weninger M, Birnbacher R, Deutinger J, Bernaschek G. Blaicher W, et al. Among authors: bernaschek g. Ultraschall Med. 2005 Feb;26(1):29-35. doi: 10.1055/s-2004-813382. Ultraschall Med. 2005. PMID: 15700225
Fetal skeletal deformities - the diagnostic accuracy of prenatal ultrasonography and fetal magnetic resonance imaging.
Blaicher W, Mittermayer C, Messerschmidt A, Deutinger J, Bernaschek G, Prayer D. Blaicher W, et al. Among authors: bernaschek g. Ultraschall Med. 2004 Jun;25(3):195-9. doi: 10.1055/s-2004-812946. Ultraschall Med. 2004. PMID: 15146359
[Prenatal diagnosis of full, non mosaic trisomy 22 in the third trimester].
Bettelheim D, Eppel W, Deutinger J, Bernaschek G. Bettelheim D, et al. Among authors: bernaschek g. Ultraschall Med. 2001 Oct;22(5):241-4. doi: 10.1055/s-2001-17895. Ultraschall Med. 2001. PMID: 11607894 German.
Combined prenatal ultrasound and magnetic resonance imaging in two fetuses with suspected arachnoid cysts.
Blaicher W, Prayer D, Kuhle S, Deutinger J, Bernaschek G. Blaicher W, et al. Among authors: bernaschek g. Ultrasound Obstet Gynecol. 2001 Aug;18(2):166-8. doi: 10.1046/j.1469-0705.2001.00503.x. Ultrasound Obstet Gynecol. 2001. PMID: 11530000
Absence of microdeletions in the azoospermia-factor region of the Y-chromosome in Viennese men seeking assisted reproduction.
Gruber CJ, Hengstschläger M, Wieser F, Gruber DM, Walch K, Ferlitsch K, Gruber IM, Maar A, Marton E, Bernaschek G, Huber JC. Gruber CJ, et al. Among authors: bernaschek g. Wien Klin Wochenschr. 2003 Dec 15;115(23):831-4. doi: 10.1007/BF03041043. Wien Klin Wochenschr. 2003. PMID: 14740346
Subtelomeric rearrangements as neutral genomic polymorphisms.
Hengstschläger M, Prusa A, Repa C, Deutinger J, Pollak A, Bernaschek G. Hengstschläger M, et al. Among authors: bernaschek g. Am J Med Genet A. 2005 Feb 15;133A(1):48-52. doi: 10.1002/ajmg.a.30520. Am J Med Genet A. 2005. PMID: 15637704 Review.
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