A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.

Peter Holmquist

Research output: Contribution to journal › Article › peer-review

Subject classification (UKÄ)

@article{d25fef61013e49a7b34f6ddbcd134f06,

title = "A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1.",

author = "Peter Holmquist",

year = "2015",

doi = "10.1097/MCD.0000000000000070",

language = "English",

volume = "24",

pages = "75--78",

journal = "Clinical Dysmorphology",

issn = "1473-5717",

publisher = "Lippincott Williams & Wilkins",

number = "2",

}