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Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).
Prenat Diagn. 2001 Dec;21(12):1049-52. doi: 10.1002/pd.192.
Prenat Diagn. 2001.
PMID: 11746162
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpoints.
Manvelyan M, Schreyer I, Höls-Herpertz I, Köhler S, Niemann R, Hehr U, Belitz B, Bartels I, Götz J, Huhle D, Kossakiewicz M, Tittelbach H, Neubauer S, Polityko A, Mazauric ML, Wegner R, Stumm M, Küpferling P, Süss F, Kunze H, Weise A, Liehr T, Mrasek K.
Manvelyan M, et al. Among authors: kossakiewicz m.
Int J Mol Med. 2007 Jun;19(6):855-64. doi: 10.3892/ijmm.19.6.855.
Int J Mol Med. 2007.
PMID: 17487417
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Pericentric inversions of the X chromosome. A new observation and review of the published cases.
Pfeiffer RA, Kossakiewicz M, Baisch C.
Pfeiffer RA, et al. Among authors: kossakiewicz m.
J Genet Hum. 1986 Aug;34(3-4):331-7.
J Genet Hum. 1986.
PMID: 3760837
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Examination of a first-trimester Down syndrome screening concept on a mix of 11,107 high- and low-risk patients at a private center for prenatal medicine in Germany.
Schaelike M, Kossakiewicz M, Kossakiewicz A, Schild RL.
Schaelike M, et al. Among authors: kossakiewicz m.
Eur J Obstet Gynecol Reprod Biol. 2009 Jun;144(2):140-5. doi: 10.1016/j.ejogrb.2009.03.007. Epub 2009 Apr 11.
Eur J Obstet Gynecol Reprod Biol. 2009.
PMID: 19362411
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