Starke H - Search Results

1

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect.

Barber JC, Zhang S, Friend N, Collins AL, Maloney VK, Hastings R, Farren B, Barnicoat A, Polityko AD, Rumyantseva NV, Starke H, Ye S. Barber JC, et al. Among authors: starke h. Cytogenet Genome Res. 2006;114(3-4):351-8. doi: 10.1159/000094225. Cytogenet Genome Res. 2006. PMID: 16954678

2

Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.

Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S. Polityko A, et al. Among authors: starke h. Cytogenet Genome Res. 2005;111(2):171-4. doi: 10.1159/000086388. Cytogenet Genome Res. 2005. PMID: 16103660

3

Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.

Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, Sanchís A, Vermeesch JR, Ramel C, Polityko A, Haas OA, Anderson J, Claussen U, von Eggeling F, Starke H. Liehr T, et al. Among authors: starke h. Cytogenet Genome Res. 2006;112(1-2):23-34. doi: 10.1159/000087510. Cytogenet Genome Res. 2006. PMID: 16276087

4

Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.

Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H. Polityko A, et al. Among authors: starke h. Int J Mol Med. 2004 Dec;14(6):977-9. Int J Mol Med. 2004. PMID: 15547662

5

Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Vermeesch JR, et al. Among authors: starke h. Eur J Med Genet. 2005 Jul-Sep;48(3):319-27. doi: 10.1016/j.ejmg.2005.04.018. Eur J Med Genet. 2005. PMID: 16179227

6

A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].

Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schöning M, Dufke A. Grasshoff U, et al. Among authors: starke h. Cytogenet Genome Res. 2003;103(1-2):17-23. doi: 10.1159/000076282. Cytogenet Genome Res. 2003. PMID: 15004458

7

Small supernumerary marker chromosomes (sSMC) in humans.

Liehr T, Claussen U, Starke H. Liehr T, et al. Among authors: starke h. Cytogenet Genome Res. 2004;107(1-2):55-67. doi: 10.1159/000079572. Cytogenet Genome Res. 2004. PMID: 15305057 Review.

8

De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.

Dufke A, Singer S, Borell-Kost S, Stotter M, Pflumm DA, Mau-Holzmann UA, Starke H, Mrasek K, Enders H. Dufke A, et al. Among authors: starke h. Cytogenet Genome Res. 2006;114(3-4):342-50. doi: 10.1159/000094224. Cytogenet Genome Res. 2006. PMID: 16954677

9

Array painting using microdissected chromosomes to map chromosomal breakpoints.

Backx L, Van Esch H, Melotte C, Kosyakova N, Starke H, Frijns JP, Liehr T, Vermeesch JR. Backx L, et al. Among authors: starke h. Cytogenet Genome Res. 2007;116(3):158-66. doi: 10.1159/000098181. Cytogenet Genome Res. 2007. PMID: 17317954

10

A molecular cytogenetic study of chromosome evolution in chimpanzee.

Gross M, Starke H, Trifonov V, Claussen U, Liehr T, Weise A. Gross M, et al. Among authors: starke h. Cytogenet Genome Res. 2006;112(1-2):67-75. doi: 10.1159/000087515. Cytogenet Genome Res. 2006. PMID: 16276092

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

153 results

Search Page

Filters