(Q37826794)

English

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy

scientific article published on January 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

1 reference

Europe PubMed Central

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

myoclonic epilepsy

1 reference

based on heuristic

inferred from title

juvenile myoclonic epilepsy

1 reference

based on heuristic

inferred from title

childhood absence epilepsy

1 reference

based on heuristic

inferred from title

5

object named as

Treiman L

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

author name string

Delgado-Escueta AV

1

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Greenberg D

2

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Weissbecker K

3

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Liu A

4

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Sparkes R

6

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Park MS

7

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Barbetti A

8

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Terasaki PI

9

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

publication date

1 January 1990

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

31 Suppl 3

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

S19-29

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Chromosome crawling in the MHC.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Construction of a general human chromosome jumping library, with application to cystic fibrosis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Bipolar affective disorders linked to DNA markers on chromosome 11

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Construction and use of human chromosome jumping libraries from NotI-digested DNA.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Human major histocompatibility complex contains a minimum of 19 genes between the complement cluster and HLA-B

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

A giant locus for the Duchenne and Becker muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Cellular Actions of Petit Mal Anticonvulsants: Implication of Thalamic Low-Threshold Calcium Current in Generation of Spike-Wave Discharge

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Physiology of Thalamic Relay Neurons: Properties of Calcium Currents Involved in Burst-Firing

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1990.TB05855.X

21 January 2018

Identifiers

10.1111/J.1528-1157.1990.TB05855.X

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

ResearchGate publication ID

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