Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations-Reference-Cited by-同舟云学术

Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations

Published:2017-08-04 Issue:1 Volume:10 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Šumanović-Glamuzina Darinka,Lozić Bernarda,Iwanowski Piotr S.,Zemunik Tatijana,Bilinovac Zeljka,Stasiewicz-Jarocka Beata,Panasiuk Barbara,Midro Alina T.

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-017-0330-8.pdf

Reference34 articles.

1. Battaglia A, Carey JC, South ST. Wolf-Hirschhorn syndrome: a review and update. Am J Med Genet C Semin Med Genet. 2015;169(3):216–23.

2. Iwanowski P, Panasiuk B, Van Buggenhout G, Murdolo M, Myśliwiec M, Maas N, Lattante S, Korniszewski L, Posmyk R, Pilch J, Zajączek S, Fryns JP, Zollino M, Midro AT. Wolf-Hirschhorn Sydrome due to pure and translocation form of Monosomy 4p16.1→pter. Am J Med Genet A. 2011;155:1833–47.

3. Maas NM, Van Buggenhout G, Hannes F, Thienpont B, Sanlaville D, Kok K, Midro A, Andrieux J, Anderlid BM, Schoumans J, Hordijk R, Devriendt K, Fryns JP, Vermeesch JR. Genotype-phenotype correlation in 21 patients with wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH). J Med Genet. 2008;45(2):71–80.

4. Zollino M, Murdolo M, Marangi G, Pecile V, Galasso C, Mazzanti L, Neri G. On the nosology and pathogenesis of wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review. Am J Med Genet C Semin Med Genet. 2008;148C(4):257–69.

5. Midro AT, Zollino M, Wiland E, Panasiuk B, Iwanowski PS, Murdolo M, Śmigiel R, Sąsiadek M, Pilch J, Kurpisz M. Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1. J Assist Reprod Genet. 2016;33(2):189–97.