Hengstschläger M - Search Results

1

[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene].

Bauer JW, Ortiz S, Hengstschläger M, Pulkkinen L, Uitto J, Hintner H, Rappersberger K. Bauer JW, et al. Among authors: hengstschlager m. Hautarzt. 1999 Feb;50(2):121-6. doi: 10.1007/s001050050875. Hautarzt. 1999. PMID: 10097955 German.

2

[Prenatal diagnosis of Bourneville-Pringle disease (cerebral tuberous sclerosis)].

Stümpflen-Mauser I, Hengstschläger M, Wimmer M, Zekert M, Bettelheim D. Stümpflen-Mauser I, et al. Among authors: hengstschlager m. Ultraschall Med. 1996 Feb;17(1):34-7. doi: 10.1055/s-2007-1000452. Ultraschall Med. 1996. PMID: 8650521 Review. German.

3

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

4

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.

5

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

6

Dandy-Walker malformation as sonographic marker for fetal triploidy.

Blaicher W, Ulm B, Ulm MR, Hengstschläger M, Deutinger J, Bernaschek G. Blaicher W, et al. Among authors: hengstschlager m. Ultraschall Med. 2002 Apr;23(2):129-33. doi: 10.1055/s-2002-25189. Ultraschall Med. 2002. PMID: 11961728

7

Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts.

Hengstschläger M, Bettelheim D, Rosner M, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Prenat Diagn. 2001 Oct;21(10):897-9. doi: 10.1002/pd.154. Prenat Diagn. 2001. PMID: 11746140 No abstract available.

8

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

9

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.

10

Neurogenic cells in human amniotic fluid.

Prusa AR, Marton E, Rosner M, Bettelheim D, Lubec G, Pollack A, Bernaschek G, Hengstschläger M. Prusa AR, et al. Among authors: hengstschlager m. Am J Obstet Gynecol. 2004 Jul;191(1):309-14. doi: 10.1016/j.ajog.2003.12.014. Am J Obstet Gynecol. 2004. PMID: 15295384

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