Müller-Navia J - Search Results

1

Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities.

Müller-Navia J, Nebel A, Oehler D, Theile U, Zabel B, Schleiermacher E. Müller-Navia J, et al. Prenat Diagn. 1996 Oct;16(10):915-22. doi: 10.1002/(SICI)1097-0223(199610)16:10<915::AID-PD966>3.0.CO;2-V. Prenat Diagn. 1996. PMID: 8938060

2

Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis.

Müller-Navia J, Nebel A, Schleiermacher E. Müller-Navia J, et al. Hum Genet. 1995 Dec;96(6):661-7. doi: 10.1007/BF00210295. Hum Genet. 1995. PMID: 8522323

3

Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.

Eggermann T, Engels H, Moskalonek B, Nöthen MM, Müller-Navia J, Schleiermacher E, Schwanitz G, Stengel-Rutkowski S. Eggermann T, et al. Hum Genet. 1996 May;97(5):568-72. doi: 10.1007/BF02281862. Hum Genet. 1996. PMID: 8655132

4

Interstitial deletion del(10)(q25.2q25.3 approximately 26.11)--case report and review of the literature.

Kehrer-Sawatzki H, Daumiller E, Müller-Navia J, Kendziorra H, Rossier E, du Bois G, Barbi G. Kehrer-Sawatzki H, et al. Among authors: muller navia j. Prenat Diagn. 2005 Oct;25(10):954-9. doi: 10.1002/pd.1252. Prenat Diagn. 2005. PMID: 16088867 Review.

5

Multiplex-FISH for pre- and postnatal diagnostic applications.

Uhrig S, Schuffenhauer S, Fauth C, Wirtz A, Daumer-Haas C, Apacik C, Cohen M, Müller-Navia J, Cremer T, Murken J, Speicher MR. Uhrig S, et al. Among authors: muller navia j. Am J Hum Genet. 1999 Aug;65(2):448-62. doi: 10.1086/302508. Am J Hum Genet. 1999. PMID: 10417288 Free PMC article.

6

Tetrasomy 18p caused by paternal meiotic nondisjunction.

Eggermann T, Engels H, Apacik C, Moskalonek B, Müller-Navia J, Schwanitz G, Stengel-Rutkowski S. Eggermann T, et al. Eur J Hum Genet. 1997 May-Jun;5(3):175-7. Eur J Hum Genet. 1997. PMID: 9272743 No abstract available.

7

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. Among authors: muller navia j. Am J Med Genet. 1999 Dec 3;87(4):297-301. Am J Med Genet. 1999. PMID: 10588833 Review.

8

A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.

Mrasek K, Krüger G, Bauer I, Müller-Navia J, Liehr T, Weise A. Mrasek K, et al. Among authors: muller navia j. Cytogenet Genome Res. 2008;121(3-4):286-7. doi: 10.1159/000138899. Epub 2008 Aug 29. Cytogenet Genome Res. 2008. PMID: 18758173

9

Chromosomal homeologies between human, harbor seal (Phoca vitulina) and the putative ancestral carnivore karyotype revealed by Zoo-FISH.

Frönicke L, Müller-Navia J, Romanakis K, Scherthan H. Frönicke L, et al. Among authors: muller navia j. Chromosoma. 1997 Jul;106(2):108-13. doi: 10.1007/s004120050230. Chromosoma. 1997. PMID: 9215560

10

Clustering of pericentromeres initiates in step 9 of spermiogenesis of the rat (Rattus norvegicus) and contributes to a well defined genome architecture in the sperm nucleus.

Meyer-Ficca M, Müller-Navia J, Scherthan H. Meyer-Ficca M, et al. Among authors: muller navia j. J Cell Sci. 1998 May;111 ( Pt 10):1363-70. doi: 10.1242/jcs.111.10.1363. J Cell Sci. 1998. PMID: 9570754

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