Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2

Yazar: TROST, D., WIEBE, W., UHLHAAS, S., SCHWINDT, P., SCHWANITZ, G.
Baskı/Yayın Bilgisi 2000

Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unb...

Yazar: Wieczorek, D, Engels, H, Viersbach, R, Henke, B, Schwanitz, G, Passarge, E
Baskı/Yayın Bilgisi 1998

Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.

Yazar: Horsthemke, B, Maat-Kievit, A, Sleegers, E, van den Ouweland, A, Buiting, K, Lich, C, Mollevanger, P, Beverstock, G, Gillessen-Kaesbach, G, Schwanitz, G
Baskı/Yayın Bilgisi 1996