Froster UG - Search Results

1

First-trimester increased nuchal translucency as a prenatal sign of Zellweger syndrome.

Strenge S, Froster UG, Wanders RJ, Gartner J, Maier EM, Muntau AC, Faber R. Strenge S, et al. Among authors: froster ug. Prenat Diagn. 2004 Feb;24(2):151-3. doi: 10.1002/pd.805. Prenat Diagn. 2004. PMID: 14974126 No abstract available.

2

Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findings.

Froster UG, Horn LC, Holland H, Strenge S, Faber R. Froster UG, et al. Prenat Diagn. 2000 Dec;20(12):992-5. doi: 10.1002/1097-0223(200012)20:12<992::aid-pd950>3.0.co;2-7. Prenat Diagn. 2000. PMID: 11113912

3

Pitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin gene.

Vondran S, Edelmann J, Holland H, Wolf C, Strenge S, Thamm B, Thiele H, Froster UG. Vondran S, et al. Among authors: froster ug. Prenat Diagn. 1999 Jan;19(1):64-7. doi: 10.1002/(sici)1097-0223(199901)19:1<64::aid-pd464>3.0.co;2-z. Prenat Diagn. 1999. PMID: 10073911

4

Prenatal detection of a giant bilateral thoracic vascular lesion: prognostic evaluation and genetic aspects.

Meiner A, Faber R, Horn LC, Reichenbach H, Froster UG. Meiner A, et al. Among authors: froster ug. Prenat Diagn. 1999 Jun;19(6):583-6. doi: 10.1002/(sici)1097-0223(199906)19:6<583::aid-pd585>3.0.co;2-b. Prenat Diagn. 1999. PMID: 10416979

5

Another case of autosomal dominant exstrophy of the bladder.

Froster UG, Heinritz W, Bennek J, Horn LC, Faber R. Froster UG, et al. Prenat Diagn. 2004 May;24(5):375-7. doi: 10.1002/pd.879. Prenat Diagn. 2004. PMID: 15164413

6

Tetraploidy in a growth-retarded fetus with a thick placenta.

Meiner A, Holland H, Reichenbach H, Horn LC, Faber R, Froster UG. Meiner A, et al. Among authors: froster ug. Prenat Diagn. 1998 Aug;18(8):864-5. Prenat Diagn. 1998. PMID: 9742582 No abstract available.

7

Potential errors with rapid analysis techniques: partial duplication 21q resulting from a paternal paracentric insertion uncovered in chorionic villus sampling by fluorescence in situ hybridization.

Ehrhardt N, Kujat A, Faber R, Horn LC, Froster UG. Ehrhardt N, et al. Among authors: froster ug. Fetal Diagn Ther. 2009;26(4):219-22. doi: 10.1159/000265555. Epub 2009 Dec 17. Fetal Diagn Ther. 2009. PMID: 20029221

8

Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I.

Kujat A, Veith VP, Faber R, Froster UG. Kujat A, et al. Among authors: froster ug. Fetal Diagn Ther. 2007;22(2):155-8. doi: 10.1159/000097117. Epub 2006 Nov 28. Fetal Diagn Ther. 2007. PMID: 17139175

9

Diaphragmatic hernia in 18p- syndrome.

Strenge S, Froster UG. Strenge S, et al. Among authors: froster ug. Am J Med Genet A. 2004 Feb 15;125A(1):97-9. doi: 10.1002/ajmg.a.20459. Am J Med Genet A. 2004. PMID: 14755475 Review. No abstract available.

10

Microcephaly-lymphedema syndrome: report of a family with short stature as additional manifestation.

Strenge S, Froster UG. Strenge S, et al. Among authors: froster ug. Am J Med Genet. 1998 Dec 28;80(5):506-9. doi: 10.1002/(sici)1096-8628(19981228)80:5<506::aid-ajmg13>3.0.co;2-1. Am J Med Genet. 1998. PMID: 9880217

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