Anwar Baban

Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association

Alpelisib for PIK3CA -Mutated, Hormone Receptor–Positive Advanced Breast Cancer

Uterine rudiments in patients with Mayer-Rokitansky-Küster-Hauser syndrome consist of typical uterine tissue types with predominantly basalis-like endometrium

The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans

The ground state of embryonic stem cell self-renewal

22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features

REPuter: the manifold applications of repeat analysis on a genomic scale

High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia

The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies

22q11.2 deletion syndrome

The Fibroblast Growth Factor signaling pathway

Management of Acute Myocarditis and Chronic Inflammatory Cardiomyopathy

AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome

Metabolic reprogramming and cancer progression

Conditional Deletion of Focal Adhesion Kinase Leads to Defects in Ventricular Septation and Outflow Tract Alignment

Phosphatidylinositol 3-Kinase, Growth Disorders, and Cancer

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome

Syndromic non‐compaction of the left ventricle: associated chromosomal anomalies