A girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient.

scientific article published on January 2007

A girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/GTE.2006.9995
P698PubMed publication ID17394389
P5875ResearchGate publication ID51377795

P50authorTaosheng HuangQ74605870
P2093author name stringAlicia Vaglio
Andrea Quadrelli
Búrix Mechoso
Roberto Quadrelli
Yao-Shan Fan
Mariela Larrandaburu
Eugen M Strehle
P433issue1
P921main subjectoccipital encephaloceleQ55786793
P304page(s)4-10
P577publication date2007-01-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleA girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient
P478volume11

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cites work (P2860)
Q4232438912-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes
Q36377807A familial deletion 4q syndrome: An outcome of a paracentric inversion
Q37053299Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy
Q51922364Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.
Q35046265Occipital meningoencephalocele with Cleft Lip, Cleft Palate and Limb Abnormalities- A Case Report
Q33828795Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

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