Midro AT - Search Results

1

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.

Midro AT, Panasiuk B, Tümer Z, Stankiewicz P, Silahtaroglu A, Lupski JR, Zemanova Z, Stasiewicz-Jarocka B, Hubert E, Tarasów E, Famulski W, Zadrozna-Tołwińska B, Wasilewska E, Kirchhoff M, Kalscheuer V, Michalova K, Tommerup N. Midro AT, et al. Am J Med Genet A. 2004 Jan 15;124A(2):179-91. doi: 10.1002/ajmg.a.20367. Am J Med Genet A. 2004. PMID: 14699618 Review.

2

Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa.

Midro AT, Wiland E, Panasiuk B, Leśniewicz R, Kurpisz M. Midro AT, et al. Am J Med Genet A. 2006 Feb 1;140(3):245-56. doi: 10.1002/ajmg.a.31083. Am J Med Genet A. 2006. PMID: 16411217

3

Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother.

Panasiuk B, Midro AT, Zadrozna-Tołwińska B. Panasiuk B, et al. Among authors: midro at. Clin Genet. 1997 Aug;52(2):120-5. doi: 10.1111/j.1399-0004.1997.tb02529.x. Clin Genet. 1997. PMID: 9298748

4

Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.

Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT. Panasiuk B, et al. Among authors: midro at. Ann Genet. 2004 Jan-Mar;47(1):11-28. doi: 10.1016/j.anngen.2004.01.001. Ann Genet. 2004. PMID: 15050871

5

Midro AT, Stasiewicz-Jarocka B, Borys J, Hubert E, Skotnicka B, Hassmann-Poznańska E, Sierpińska T, Panasiuk B, Schanze D, Zenker M. Midro AT, et al. Am J Med Genet A. 2020 Apr;182(4):773-779. doi: 10.1002/ajmg.a.61495. Epub 2020 Jan 30. Am J Med Genet A. 2020. PMID: 31999076

6

A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.

Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT. Posmyk R, et al. Among authors: midro at. Genet Couns. 2005;16(1):17-25. Genet Couns. 2005. PMID: 15844774

7

Familial occurrence of isodicentric X chromosomes with different breakpoints.

Midro AT, Kulikowski M, Sawicka A, Panasiuk B, Korsak E. Midro AT, et al. Clin Genet. 1988 Sep;34(3):153-60. doi: 10.1111/j.1399-0004.1988.tb02855.x. Clin Genet. 1988. PMID: 3180502

8

Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

Midro AT, Panasiuk B, Stasiewicz-Jarocka B, Olszewska M, Wiland E, Myśliwiec M, Kurpisz M, Shaffer LG, Gajecka M. Midro AT, et al. J Hum Genet. 2014 Dec;59(12):667-74. doi: 10.1038/jhg.2014.92. Epub 2014 Oct 16. J Hum Genet. 2014. PMID: 25319850

9

Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.

Iwanowski PS, Panasiuk B, Van Buggenhout G, Murdolo M, Myśliwiec M, Maas NM, Lattante S, Korniszewski L, Posmyk R, Pilch J, Zajączek S, Fryns JP, Zollino M, Midro AT. Iwanowski PS, et al. Among authors: midro at. Am J Med Genet A. 2011 Aug;155A(8):1833-47. doi: 10.1002/ajmg.a.34005. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744486

10

[Risk estimation of different pregnancy outcomes in the families of carriers of reciprocal chromosomal translocations involving chromosome 20].

Stasiewicz-Jarocka B, Kozaczuk M, Panasiuk B, Jamsheer A, Latos-Bieleńska A, Midro AT. Stasiewicz-Jarocka B, et al. Among authors: midro at. Ginekol Pol. 2013 Jun;84(6):422-9. doi: 10.17772/gp/1599. Ginekol Pol. 2013. PMID: 24032259 Polish.

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