Benign Familial Neonatal Convulsions

Benign Familial Neonatal Convulsions

Linkage studies with the chromosome 20 markers D20S19 and D20S20 were performed in two families with benign familial neonatal convulsions at the Department of Pediatrics, The University of Texas Health Science Center, San Antonio, TX.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 1991-06-01
Series:Pediatric Neurology Briefs
Subjects:
dominant primary epilepsy
genetically heterogeneous
late adolescence
Online Access:https://www.pediatricneurologybriefs.com/articles/3256
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spelling doaj-d1499def2f314a469ddaf4e7df6645222020-11-25T03:03:59ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64821991-06-0156474710.15844/pedneurbriefs-5-6-103242Benign Familial Neonatal ConvulsionsJ Gordon Millichap0Northwestern University Feinberg School of MedicineLinkage studies with the chromosome 20 markers D20S19 and D20S20 were performed in two families with benign familial neonatal convulsions at the Department of Pediatrics, The University of Texas Health Science Center, San Antonio, TX.https://www.pediatricneurologybriefs.com/articles/3256dominant primary epilepsygenetically heterogeneouslate adolescence
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
Benign Familial Neonatal Convulsions
Pediatric Neurology Briefs
dominant primary epilepsy
genetically heterogeneous
late adolescence
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title Benign Familial Neonatal Convulsions
title_short Benign Familial Neonatal Convulsions
title_full Benign Familial Neonatal Convulsions
title_fullStr Benign Familial Neonatal Convulsions
title_full_unstemmed Benign Familial Neonatal Convulsions
title_sort benign familial neonatal convulsions
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 1991-06-01
description Linkage studies with the chromosome 20 markers D20S19 and D20S20 were performed in two families with benign familial neonatal convulsions at the Department of Pediatrics, The University of Texas Health Science Center, San Antonio, TX.
topic dominant primary epilepsy
genetically heterogeneous
late adolescence
url https://www.pediatricneurologybriefs.com/articles/3256
work_keys_str_mv AT jgordonmillichap benignfamilialneonatalconvulsions
_version_ 1724683551140478976

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