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Digenic inheritance

A type of multifactorial inheritance governed by the simultaneous action of two gene loci. [HPO:probinson, ISBN:978-0192628961]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Genetic and clinical findings of panel‐based targeted exome sequencing in a northeast Chinese cohort with retinitis pigmentosa
Panel‐based targeted exome sequencing was used to analyze the genetic and clinical findings of targeted genes in a cohort of… 
2019
2019
Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique
Alport syndrome (AS) is an inherited progressive renal disease caused by mutations in COL4A3, COL4A4, and COL4A5 genes. The large… 
Review
2018
Review
2018
A new leaf rust resistance gene Lr79 mapped in chromosome 3BL from the durum wheat landrace Aus26582
A new leaf rust resistance gene Lr79 has been mapped in the long arm of chromosome 3B and a linked marker was identified for… 
Review
2017
Review
2017
Alport syndrome: impact of digenic inheritance in patients management
Alport syndrome (ATS) is a genetically heterogeneous nephropathy with considerable phenotypic variability and different… 
Highly Cited
2015
Highly Cited
2015
Mutations in CDK5RAP2 cause Seckel syndrome
Seckel syndrome is a heterogeneous, autosomal recessive disorder marked by prenatal proportionate short stature, severe… 
2011
2011
Searching for digenic inheritance in deaf Brazilian individuals using the multiplex ligation-dependent probe amplification technique.
Mutations in the genes coding for connexin 26 (Cx26), connexin 30 (Cx30), and connexin 31 (Cx31) are the main cause of autosomal… 
Highly Cited
2008
Highly Cited
2008
Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.
Kallmann syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia or hyposmia. To date, 4… 
Review
2007
Review
2007
Multiple mutations responsible for frequent genetic diseases in isolated populations
The relatively frequent existence of an autosomal recessive disease in an isolated population suggests a founder effect. However… 
Highly Cited
2000
Highly Cited
2000
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?
The Antley-Bixler syndrome has been thought to be caused by an autosomal recessive gene. However, patients with this phenotype… 
1996
1996
CONFIRMATION OF DIGENIC INHERITANCE OF COTYLEDON COLOUR IN LENTIL (LENS CULINARIS)
The F3 seeds harvested from F2 populations of five crosses between parents with orange and light green cotyledons were analysed… 
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