12q11-q13

A chromosome band present on 12q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1991-2014
012319912014

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2014
2014
Monilethrix is generally considered to be an autosomal-dominant disorder with variable penetrance. It is caused by mutations of… (More)
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2007
2007
We analyzed a cohort of 61 follicular lymphomas (FL) with an abnormal G-banded karyotype by spectral karyotyping (SKY) to better… (More)
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1999
1999
Diffuse non-epidermolytic palmoplantar keratoderma (NEPPK) belongs to the heterogeneous group of skin diseases characterized by… (More)
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1998
1998
Human hHb1 belongs to the type II hard keratin family and is physiologically expressed in hair shafts. In the present study… (More)
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1996
1996
Monilethrix is characterized by beaded or moniliform hair, which results from the periodic thinning of the hair shaft. The beaded… (More)
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1996
1996
Epidermolysis bullosa simplex (EBS) is a group of autosomal dominant skin diseases characterized by blistering, due to mechanical… (More)
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1996
1996
Mapping studies of functional keratin genes in the human genome have localized most of the acidic keratin genes to chromosome… (More)
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1994
1994
Hereditary palmoplantar keratoderma is characterized by hyperkeratosis of the skin of palms and soles. An autosomal dominant form… (More)
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1993
1993
Epidermolysis bullosa simplex (EBS) is a group of autosomal dominant skin diseases characterized by blistering, due to mechanical… (More)
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1991
1991
Epidermolysis bullosa simplex (EBS) is a dominantly inherited genodermatosis characterized by intraepidermal blister formation… (More)
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