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

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Review
2018
Review
2018
Digenic inheritance (DI) concerns pathologies with the simplest form of multigenic etiology, implicating more than 1 gene (and… (More)
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Review
2013
Review
2013
Digenic inheritance (DI) is the simplest form of inheritance for genetically complex diseases. By contrast with the thousands of… (More)
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Usher syndrome (USH) is an autosomal recessive disorder comprising retinitis pigmentosa, hearing loss and, in some… (More)
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2011
2011
Hypotrichosis is a human hereditary hair loss disorder in which affected individuals show sparse to complete absence of hair on… (More)
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2011
2011
Mutations in the genes coding for connexin 26 (Cx26), connexin 30 (Cx30), and connexin 31 (Cx31) are the main cause of autosomal… (More)
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2008
2008
Kallmann syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia or hyposmia. To date, 4… (More)
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2000
2000
The Antley-Bixler syndrome has been thought to be caused by an autosomal recessive gene. However, patients with this phenotype… (More)
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1998
1998
We investigated a Swedish family with nonsyndromic progressive bilateral sensorineural hearing loss. Thirteen candidate loci for… (More)
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1996
1996
The F3 seeds harvested from F2 populations of five crosses between parents with orange and light green cotyledons were analysed… (More)
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1969
1969
Gynodioecy is an outbreeding mechanism where both male-sterile (i.e. female) and hermaphrodite plants are found. Plantago… (More)
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