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Publications by Michael Graef
Two Patients With the Heterozygous R189H Mutation in ACTA2 and Complex Congenital Heart Defects Expands the Cardiac Phenotype of Multisystemic Smooth Muscle Dysfunction Syndrome
American Journal of Medical Genetics, Part A
Genetics
RESITA Network: Academic Entrepreneurship and Innovation Network of South Eastern European Universities: An Example of Successful Networking in Entrepreneurship and Innovation at Academic Level
Serbian Journal of Management
Accounting
Management
Business
Related publications
Prevalence of Congenital Heart Defects in Patients With Down’s Syndrome
Jornal de Pediatria
Child Health
Pediatrics
Perinatology
Congenital Heart Defects Are Under-Recognised in Adult Patients With Down's Syndrome
Heart
Cardiovascular Medicine
Cardiology
MESP1 Mutations in Patients With Congenital Heart Defects
Human Mutation
Genetics
Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart Defects
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Phenotype and Genotype Report on Homozygous and Heterozygous Patients With Congenital Factor X Deficiency
Haematologica
Hematology
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation
Genetics in Medicine
Medicine
Genetics
Rare Copy Number Variants Analysis Identifies Novel Candidate Genes in Heterotaxy Syndrome Patients With Congenital Heart Defects
Genome Medicine
Molecular Medicine
Genetics
Molecular Biology
Smooth Muscle Α Actin (Acta2) and Myofibroblast Function During Hepatic Wound Healing
PLoS ONE
Multidisciplinary
