TY  - GEN
AU  - Wieland,I
AU  - Weidner,C
AU  - Ciccone,R
AU  - Lapi,E
AU  - McDonald-McGinn,D
AU  - Kress,W
AU  - Jakubiczka,S
AU  - Collmann,H
AU  - Zuffardi,O
AU  - Zackai,E
AU  - Wieacker,P
TI  - Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome
SN  - 0009-9163
PY  - 2008///0122
KW  - Adolescent
KW  - Base Sequence
KW  - Child, Preschool
KW  - Craniofacial Abnormalities
KW  - genetics
KW  - Cytoskeletal Proteins
KW  - deficiency
KW  - DNA Primers
KW  - Ectodysplasins
KW  - Ephrin-B1
KW  - Female
KW  - GTPase-Activating Proteins
KW  - Gene Deletion
KW  - Genetic Diseases, X-Linked
KW  - Heterozygote
KW  - Humans
KW  - Nuclear Proteins
KW  - Phenotype
KW  - Syndrome
KW  - Ubiquitin-Protein Ligases
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/j.1399-0004.2007.00905.x
ER  -