Hengstschläger M - Search Results

1

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: hengstschlager m. 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.

2

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. Fetal Diagn Ther. 2004 Nov-Dec;19(6):510-2. doi: 10.1159/000080164. Fetal Diagn Ther. 2004. PMID: 15539876 Review.

3

Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.

Hengstschläger M, Bettelheim D, Drahonsky R, Deutinger J, Bernaschek G. Hengstschläger M, et al. Prenat Diagn. 2001 Jun;21(6):477-80. doi: 10.1002/pd.95. Prenat Diagn. 2001. PMID: 11438953 Review.

4

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. 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.

5

A new cytofluorometric approach to detect fetal cells in the maternal circulation.

Hengstschläger M, Bernaschek G. Hengstschläger M, et al. J Med Genet. 1997 Sep;34(9):789-90. doi: 10.1136/jmg.34.9.789. J Med Genet. 1997. PMID: 9321773 Free PMC article. No abstract available.

6

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. 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.

7

Prenatal diagnosis of a supernumerary aberrant chromosome 9.

Hengstschläger M, Bettelheim D, Dörfler-Grassauer D, Prusa AR, Drahonsky R, Deutinger J, Bernaschek G. Hengstschläger M, et al. Arch Gynecol Obstet. 2003 Aug;268(3):248-50. doi: 10.1007/s00404-002-0355-y. Epub 2002 Sep 26. Arch Gynecol Obstet. 2003. PMID: 12942262

8

Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation.

Hengstschläger M, Bettelheim D, Drahonsky R, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Prenat Diagn. 2004 Aug;24(8):623-6. doi: 10.1002/pd.933. Prenat Diagn. 2004. PMID: 15305350

9

A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9).

Hengstschläger M, Bettelheim D, Repa C, Lang S, Deutinger J, Bernaschek G. Hengstschläger M, et al. Fetal Diagn Ther. 2002 Jul-Aug;17(4):243-6. doi: 10.1159/000063401. Fetal Diagn Ther. 2002. PMID: 12065954

10

Fetal cells in the peripheral blood of pregnant women express thymidine kinase: a new marker for detection.

Hengstschläger M, Bernaschek G. Hengstschläger M, et al. FEBS Lett. 1997 Mar 10;404(2-3):299-302. doi: 10.1016/s0014-5793(97)00144-0. FEBS Lett. 1997. PMID: 9119083 Free article.

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