Products and Services
PubMed/MEDLINE
MeSH
UMLS
MedlinePlus
LocatorPlus
Digital Collections
All Products and Services
Resources for You
For Researchers
For Publishers
For Librarians
For Educators/Trainers
For Healthcare Professionals
For the Public
Explore NLM
Using The Library
About The Library
History of Medicine
Programs & Initiatives
Grants and Funding
Grant Programs
Grant Deadlines
Frequently Asked Questions (FAQ)
University-based Training Programs
NIH Pathway to Independence Award
Search help
Search Web Archives
All Results
Health Information
Programs & Services
Exhibits & Collections
Refine results by
All Results
Health Information
Programs & Services
Exhibits & Collections
4
results
Cantú Syndrome and Related Disorders - GeneReviews® - NCBI Bookshelf
... terminalis with gingival hyperplasia has been linked to
17q24.2
-q24.3 [ Sun et al 2009 ]; thus, this ... D, et al. Copy-number mutations on chromosome
17q24.2
-q24.3 in congenital generalized hypertrichosis terminalis with ...
Most Recent PubMed Articles
Association of
17q24.2
-q24.3
deletions with
recognizable
phenotype and short telomeres.
Prenatal
Diagnosis of a 2.5 Mb De Novo
17q24
.1q24.
2
Deletion Encompassing KPNA2 and PSMD12 Genes in a
Fetus
with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly.
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and
Speech
Delay,
Postnatal
Microcephaly, and Dysmorphic Features.
More articles »
