TY  - GEN
AU  - Orstavik,K H
AU  - Tangsrud,S E
AU  - Nordshus,T
AU  - Lange,J E
AU  - Renolen,O
AU  - Lyberg,T
TI  - Severe craniofacial malformations and deglutition dysfunction in a brother and sister: new syndrome?
SN  - 0148-7299
PY  - 1998///0923
KW  - Abnormalities, Multiple
KW  - classification
KW  - Birth Weight
KW  - Cleft Palate
KW  - genetics
KW  - Craniofacial Abnormalities
KW  - Deglutition Disorders
KW  - Fatal Outcome
KW  - Female
KW  - Gastroesophageal Reflux
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Mosaicism
KW  - Nuclear Family
KW  - Phenotype
KW  - Polymorphism, Single-Stranded Conformational
KW  - Psychomotor Performance
KW  - Radiography
KW  - Receptor Protein-Tyrosine Kinases
KW  - Receptor, Fibroblast Growth Factor, Type 2
KW  - Receptors, Fibroblast Growth Factor
KW  - Spinal Curvatures
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/(sici)1096-8628(19980707)78:3<260::aid-ajmg10>3.0.co;2-d
ER  -