Fritz B - Search Results

1

Fetal manifestation of the Fine-Lubinsky syndrome. Brachycephaly, deafness, cataract, microstomia and mental retardation syndrome complicated by Pierre-Robin anomaly and polyhydramnios.

Schoner K, Bald R, Fritz B, Rehder H. Schoner K, et al. Among authors: fritz b. Fetal Diagn Ther. 2008;23(3):228-32. doi: 10.1159/000116746. Epub 2008 Feb 20. Fetal Diagn Ther. 2008. PMID: 18417983

2

[Possibilities for false-negative findings in trisomy 21 screening with FISH].

Fritz B, Van Oorschot B, Latta E, Rehder H. Fritz B, et al. Z Geburtshilfe Neonatol. 1996 Sep-Oct;200(5):191-8. Z Geburtshilfe Neonatol. 1996. PMID: 9035829 German.

3

Microdeletion 22q11 in complex cardiovascular malformations.

Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H. Mehraein Y, et al. Among authors: fritz b. Hum Genet. 1997 Apr;99(4):433-42. doi: 10.1007/s004390050385. Hum Genet. 1997. PMID: 9099830

4

Loss of heterozygosity of the retinoblastoma (RB1) gene in lipomas from a retinoblastoma patient.

Rieder H, Lohmann D, Poensgen B, Fritz B, Aslan M, Drohm D, Strombach Angersbach FJ, Rehder H. Rieder H, et al. Among authors: fritz b. J Natl Cancer Inst. 1998 Feb 18;90(4):324-6. doi: 10.1093/jnci/90.4.324. J Natl Cancer Inst. 1998. PMID: 9486820 No abstract available.

5

Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp.

Fritz B, Küster W, Orstavik KH, Naumova A, Spranger J, Rehder H. Fritz B, et al. Hum Genet. 1998 Oct;103(4):441-9. doi: 10.1007/s004390050848. Hum Genet. 1998. PMID: 9856488 Review.

6

Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.

Fritz B, Müller-Navia J, Hillig U, Köhler M, Aslan M, Rehder H. Fritz B, et al. Am J Med Genet. 1999 Dec 3;87(4):297-301. Am J Med Genet. 1999. PMID: 10588833 Review.

7

Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen.

Fritz B, Greber-Platzer S, Frischer T, Streubel B, Gröblacher J, Amann G, Ventruba P, Rehder H, Fonatsch C. Fritz B, et al. Am J Med Genet. 2000 Oct 2;94(4):271-80. doi: 10.1002/1096-8628(20001002)94:4<271::aid-ajmg2>3.0.co;2-y. Am J Med Genet. 2000. PMID: 11038438

8

Variability in the phenotypic expression of fryns syndrome: A report of two sibships.

Ramsing M, Gillessen-Kaesbach G, Holzgreve W, Fritz B, Rehder H. Ramsing M, et al. Among authors: fritz b. Am J Med Genet. 2000 Dec 18;95(5):415-24. doi: 10.1002/1096-8628(20001218)95:5<415::aid-ajmg2>3.0.co;2-j. Am J Med Genet. 2000. PMID: 11146459

9

Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.

Fritz B, Hallermann C, Olert J, Fuchs B, Bruns M, Aslan M, Schmidt S, Coerdt W, Müntefering H, Rehder H. Fritz B, et al. Eur J Hum Genet. 2001 Jul;9(7):539-47. doi: 10.1038/sj.ejhg.5200669. Eur J Hum Genet. 2001. PMID: 11464246

10

Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.

Bartsch C, Aslan M, Köhler J, Miny P, Horst J, Holzgreve W, Rehder H, Fritz B. Bartsch C, et al. Among authors: fritz b. Fetal Diagn Ther. 2001 Sep-Oct;16(5):265-73. doi: 10.1159/000053926. Fetal Diagn Ther. 2001. PMID: 11509847

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