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Publication | Open Access

X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes

DOIFull Paper Access

81

Citations

38

References

2014

Year

Anju K. Philips, Auli Sirén, Kristiina Avela, Mirja Somer, Maarit Peippo, Minna Ahvenainen, Fatma Doagu, Maria Arvio, Helena Kääriäinen, Hilde Van Esch,
Orphanet Journal of Rare Diseases

References

YearCitations

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