Literature DB >> 21739569

Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality.

A Nicoulaz1, F Rubi, L Lieder, R Wolf, B Goeggel-Simonetti, M Steinlin, R Wiest, H M Bonel, A Schaller, S Gallati, B Conrad.   

Abstract

Monosomy 1p36 results from heterozygous deletions of the terminal short chromosome 1 arm, the most common terminal deletion in humans. The microdeletion is split in two usually non-overlapping and clinically distinct classical distal and proximal 1p36 monosomy syndromes. Using comparative genome hybridization, MLPA and qPCR we identified the largest contiguous ∼16 Mb terminal 1p36 deletion reported to date. It covers both distal and proximal regions, causes a neonatally lethal variant with virtually exclusive features of distal 1p36 monosomy, highlighting the key importance of the gene-rich distal region for the "compound" 1p36 phenotype and a threshold deletion-size effect for haplo-lethality.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21739569     DOI: 10.1002/ajmg.a.33210

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

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

Authors:  Alina Teresa Midro; Barbara Panasiuk; Beata Stasiewicz-Jarocka; Marta Olszewska; Ewa Wiland; Marta Myśliwiec; Maciej Kurpisz; Lisa G Shaffer; Marzena Gajecka
Journal:  J Hum Genet       Date:  2014-10-16       Impact factor: 3.172

2.  De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.

Authors:  Brieana Fregeau; Bum Jun Kim; Andrés Hernández-García; Valerie K Jordan; Megan T Cho; Rhonda E Schnur; Kristin G Monaghan; Jane Juusola; Jill A Rosenfeld; Elizabeth Bhoj; Elaine H Zackai; Stephanie Sacharow; Kristin Barañano; Daniëlle G M Bosch; Bert B A de Vries; Kristin Lindstrom; Audrey Schroeder; Philip James; Peggy Kulch; Seema R Lalani; Mieke M van Haelst; Koen L I van Gassen; Ellen van Binsbergen; A James Barkovich; Daryl A Scott; Elliott H Sherr
Journal:  Am J Hum Genet       Date:  2016-04-14       Impact factor: 11.025

3.  Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.

Authors:  Hitisha P Zaveri; Tyler F Beck; Andrés Hernández-García; Katharine E Shelly; Tara Montgomery; Arie van Haeringen; Britt-Marie Anderlid; Chirag Patel; Himanshu Goel; Gunnar Houge; Bernice E Morrow; Sau Wai Cheung; Seema R Lalani; Daryl A Scott
Journal:  PLoS One       Date:  2014-01-15       Impact factor: 3.240

4.  Clinical detection of deletion structural variants in whole-genome sequences.

Authors:  Aaron C Noll; Neil A Miller; Laurie D Smith; Byunggil Yoo; Stephanie Fiedler; Linda D Cooley; Laurel K Willig; Josh E Petrikin; Julie Cakici; John Lesko; Angela Newton; Kali Detherage; Isabelle Thiffault; Carol J Saunders; Emily G Farrow; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2016-08-03       Impact factor: 8.617

5.  An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.

Authors:  Bum Jun Kim; Hitisha P Zaveri; Oleg A Shchelochkov; Zhiyin Yu; Andrés Hernández-García; Michelle L Seymour; John S Oghalai; Fred A Pereira; David W Stockton; Monica J Justice; Brendan Lee; Daryl A Scott
Journal:  PLoS One       Date:  2013-02-25       Impact factor: 3.240

Review 6.  1p36 deletion syndrome: an update.

Authors:  Valerie K Jordan; Hitisha P Zaveri; Daryl A Scott
Journal:  Appl Clin Genet       Date:  2015-08-27
  6 in total

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