The Chromosome 22q11.2 Deletion Syndrome 2022
DOI: 10.1016/b978-0-12-816047-3.00002-2
|View full text |Cite
|
Sign up to set email alerts
|

Embryonic development in 22q11.2 deletion syndrome

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 143 publications
0
1
0
Order By: Relevance
“…An expansive literature has since established Tbx1 as a key regulator of cranial development, governing aspects of the differentiation and migration of cells arising from the pharyngeal arches and neural crest (reviewed in Baldini, Fulcoli & Illingworth, 2017 ). The human phenotypes associated with Tbx1 dosage variation overlap with cat-eye syndrome and both syndromes are attributable in part to defects in pharyngeal arch development mediated by abnormal cell migration ( Tan et al, 2010 , Ivins & Scambler, 2022 ). Indeed, Tbx1 is tightly linked to the CE synteny block in human and deletions of either constitute similar subclasses of 22q11 microdeletion syndrome ( Tan et al, 2010 ), although Tbx1 is not located near either synteny block in mammals generally (see Tbx1 gene pages for taxa in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…An expansive literature has since established Tbx1 as a key regulator of cranial development, governing aspects of the differentiation and migration of cells arising from the pharyngeal arches and neural crest (reviewed in Baldini, Fulcoli & Illingworth, 2017 ). The human phenotypes associated with Tbx1 dosage variation overlap with cat-eye syndrome and both syndromes are attributable in part to defects in pharyngeal arch development mediated by abnormal cell migration ( Tan et al, 2010 , Ivins & Scambler, 2022 ). Indeed, Tbx1 is tightly linked to the CE synteny block in human and deletions of either constitute similar subclasses of 22q11 microdeletion syndrome ( Tan et al, 2010 ), although Tbx1 is not located near either synteny block in mammals generally (see Tbx1 gene pages for taxa in Fig.…”
Section: Resultsmentioning
confidence: 99%