Concepedia

Publication | Open Access

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

DOIFull Paper Access

121

Citations

30

References

2011

Year

Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K. Bijlsma, Arif B. Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki,
BMC Medical Genetics

References

YearCitations

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