TY  - GEN
AU  - Koçak,H
AU  - Ozaydin,E
AU  - Köse,G
AU  - Marcelis,C L M
AU  - Kamsteeg,E J
AU  - Ceylaner,S
TI  - A Feingold syndrome case with previously undescribed features and a new mutation
SN  - 1015-8146
PY  - 2009///1116
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Chromosome Aberrations
KW  - Craniofacial Abnormalities
KW  - Duodenum
KW  - abnormalities
KW  - Esophageal Atresia
KW  - Fingers
KW  - Genes, Dominant
KW  - genetics
KW  - Humans
KW  - Infant
KW  - Intestinal Atresia
KW  - Male
KW  - Microcephaly
KW  - Mutation, Missense
KW  - N-Myc Proto-Oncogene Protein
KW  - Nuclear Proteins
KW  - Oncogene Proteins
KW  - Phenotype
KW  - Spasms, Infantile
KW  - Syndrome
KW  - Turkey
N1  - Publication Type: Case Reports; Journal Article
ER  -