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J

J. P. Fryns

Centre For Human Genetics(IN)

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159

Papers

4.9K

Citations

30

h-index

90

i10-index

J. P. Fryns is an academic researcher from Centre For Human Genetics. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Prenatal Screening and Diagnostics & Genetics and Neurodevelopmental Disorders. The author has an h-index of 30, co-authored 136 publications.

Research Topics

Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Genetics and Neurodevelopmental Disorders Congenital limb and hand anomalies Congenital heart defects research

Papers by this author

works

Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males

2005 · European Journal of Human Genetics · 10 citations

https://doi.org/10.1038/sj.ejhg.5201399

Karine Poirier Fiona Francis Ben C.J. Hamel Claude Moraine

Research topics

topics

Genomic variations and chromosomal abnormalities

Prenatal Screening and Diagnostics

Genetics and Neurodevelopmental Disorders

Congenital limb and hand anomalies

Congenital heart defects research

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