https://www.semanticscholar.org/topic/Chromosome-1p36-Deletion-Syndrome/887812
Chromosome 1p36 Deletion Syndrome | Semantic Scholar
A rare syndrome caused by the deletion of the distal band on the short arm of chromosome 1. It is characterized by a distinctive facial appearance...
chromosomedeletionsyndromesemanticscholar
https://www.1p36.co.uk/
Home | The 1p36 Family Trust | United Kingdom
The 1p36 Family Trust is a registered charity devoted to supporting children and adults affected by 1P36 Deletion Syndrome and their families in the UK
family trustunitedkingdom
https://pubmed.ncbi.nlm.nih.gov/28428889/
Detection of 1p36 deletion by clinical exome-first diagnostic approach
Although chromosome 1p36 deletion syndrome is considered clinically recognizable based on characteristic features, the clinical manifestations of patients...
detectiondeletionclinicalexomefirst
https://pmc.ncbi.nlm.nih.gov/articles/PMC4555966/
1p36 deletion syndrome: an update - PMC
Deletions of chromosome 1p36 affect approximately 1 in 5,000 newborns and are the most common terminal deletions in humans. Medical problems commonly caused by...
an updatedeletionsyndromepmc