Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. (Q35194286)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. |
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Statements
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment (English)
J Zonana
J Gault
K J Davies
M Jones
D Browne
M Litt
N Brockdorff
S Rastan
A Clarke
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1 reference