Publications by authors named "Max Krall"

Claim this Profile
E
Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population.
Farrah Islam, Stephanie Htun, Li-Wen Lai, Max Krall, Menitha Poranki

Clin Genet· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Use of PTC124 for nonsense suppression therapy targeting BMP4 nonsense variants in vitro and the bmp4st72 allele in zebrafish.
Max Krall, Stephanie Htun, Anne Slavotinek

PLoS One· December 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies.
Max Krall, Stephanie Htun, Rhonda E Schnur, Alice S Brooks, Laura Baker

Eur J Hum Genet· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of clinical outcomes in metastatic breast cancer patients with circulating tumour cell and circulating cell-free DNA.
Zhong Ye, Chun Wang, Shaogui Wan, Zhaomei Mu, Zhenchao Zhang, Max Krall

Eur J Cancer· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome.
Anneke Kievit, Federico Tessadori, Hannie Douben, Ingrid Jordens, Madelon Maurice, Max Krall

Eur J Hum Genet· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A recurrent, non-penetrant sequence variant, p.Arg266Cys in Growth/Differentiation Factor 3 () in a female with unilateral anophthalmia and skeletal anomalies.
Tanya Bardakjian, Max Krall, Di Wu, Richard Lao, Paul Ling-Fung Tang

Am J Ophthalmol Case Rep· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expansion of phenotype and genotypic data in CRB2-related syndrome.
Ryan E Lamont, Wen-Hann Tan, A Micheil Innes, Jillian S Parboosingh, Dina Schneidman-Duhovny, Max Krall

Eur J Hum Genet· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis