Concepedia

Lyndsey Connell

LC

Statistics

Publications

2

Citations

100

H-Index

2

Active since

2011

Affiliations

Churchill Hospital(Current)

Lyndsey Connell is an author at Churchill Hospital specializing in genetic syndromes, molecular genetics, and genetics.

Publications per year

2011–2011

2

Publications

2

Compound heterozygous deletion of<i>NRXN1</i>causing severe developmental delay with early onset epilepsy in two sisters

Victoria Harrison, Lyndsey Connell, Jesse B.G. Hayesmoore et al. · American Journal of Medical Genetics Part A · 2011 · 83 citations

, , +17

Duplication of the<i>EFNB1</i>gene in familial hypertelorism: imbalance in ephrin‐B1 expression and abnormal phenotypes in humans and mice

Christian Babbs, Helen Stewart, Louise Williams et al. · Human Mutation · 2011 · 17 citations · Full text

, , +14

1–2 of 2