Back to Search
Start Over
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
- Source :
-
Journal of medical genetics [J Med Genet] 2004 May; Vol. 41 (5), pp. 381-6. - Publication Year :
- 2004
- Subjects :
- Abnormalities, Multiple metabolism
Abnormalities, Multiple pathology
Amino Acid Sequence
Embryo, Mammalian metabolism
Female
Gene Expression
Genetic Diseases, X-Linked genetics
Heart embryology
Humans
Hypertelorism diagnosis
Hypertelorism metabolism
Hypospadias diagnosis
Hypospadias metabolism
Male
Molecular Sequence Data
Myocardium metabolism
Pedigree
RNA, Messenger metabolism
Rhombencephalon embryology
Rhombencephalon metabolism
Syndrome
Ubiquitin-Protein Ligases
Abnormalities, Multiple genetics
Hypertelorism genetics
Hypospadias genetics
Microtubule Proteins genetics
Mutation
Nuclear Proteins genetics
Transcription Factors genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-6244
- Volume :
- 41
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of medical genetics
- Publication Type :
- Report
- Accession number :
- 15121778
- Full Text :
- https://doi.org/10.1136/jmg.2003.014829