Bibliographic Details
| Title: |
Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder. |
| Authors: |
Chan JCK; Department of Clinical Genetics, Hong Kong Children's Hospital, Kowloon, Hong Kong., Ho SKL, Cheng SSW, Luk HM |
| Source: |
Clinical dysmorphology [Clin Dysmorphol] 2026 Apr 01; Vol. 35 (2), pp. 74-76. Date of Electronic Publication: 2026 Feb 09. |
| Publication Type: |
Journal Article |
| Journal Info: |
Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE; In Process |
| Database: |
MEDLINE Ultimate |
