Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation-Reference-Cited by-同舟云学术

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation

Author:

Abdel-Salam Ghada M.H.¹^ORCID,Abdel-Hamid Mohamed S.²,Mehrez Mennat I.³,Kamal Ahmad M.⁴,Taher Mohamed B.¹,Afifi Hanan H.¹

Affiliation:

1. Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt

2. Medical Molecular Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt

3. Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt

4. Ophthalmology Department, Cairo University, Cairo, Egypt

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

Reference14 articles.

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