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Publications by Krisztina Németh
A Unique Haplotype of RCCX Copy Number Variation: From the Clinics of Congenital Adrenal Hyperplasia to Evolutionary Genetics
European Journal of Human Genetics
Genetics
Running in the Family – Paternalism and Familiness in the Development of Family Businesses
Vezetéstudomány / Budapest Management Review
Related publications
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
Copy Number Variation in Congenital Heart Defects
Current Genetic Medicine Reports
The Importance of Copy Number Variation in Congenital Heart Disease
npj Genomic Medicine
Genetics
Molecular Biology
Nonclassic Congenital Adrenal Hyperplasia
Current Opinion in Endocrinology, Diabetes and Obesity
Internal Medicine
Nutrition
Endocrinology
Dietetics
Medicine
Metabolism
Diabetes
Letter: Congenital Adrenal Hyperplasia.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Non-Classic Congenital Adrenal Hyperplasia
Steroids
Organic Chemistry
Molecular Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Four Clinical Variants of Congenital Adrenal Hyperplasia
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Congenital Adrenal Hyperplasia and Multiple Sclerosis
Archives of Neurology
Steroid Metabolism in a Case of Congenital Adrenal Hyperplasia
BMJ
