Pages that link to "LMX1B"
← LMX1B
Showing 50 items.
- Genetic disorder (links | edit)
- P53 (links | edit)
- Transcription factor (links | edit)
- Androgen insensitivity syndrome (links | edit)
- Homeobox (links | edit)
- FOXP2 (links | edit)
- Langer–Giedion syndrome (links | edit)
- Lissencephaly (links | edit)
- Zinc finger (links | edit)
- Cleft lip and cleft palate (links | edit)
- Septo-optic dysplasia (links | edit)
- Tietz syndrome (links | edit)
- Congenital hypothyroidism (links | edit)
- FOX proteins (links | edit)
- Rho factor (links | edit)
- Sigma factor (links | edit)
- XY gonadal dysgenesis (links | edit)
- Hormone receptor (links | edit)
- Receptor (biochemistry) (links | edit)
- Peroxisome proliferator-activated receptor (links | edit)
- Waardenburg syndrome (links | edit)
- CREB (links | edit)
- Kabuki syndrome (links | edit)
- Maturity-onset diabetes of the young (links | edit)
- Li–Fraumeni syndrome (links | edit)
- Steroid hormone receptor (links | edit)
- Helix-turn-helix (links | edit)
- Thyroid hormone resistance (links | edit)
- MyoD (links | edit)
- Oct-4 (links | edit)
- EGR1 (links | edit)
- Pickardt syndrome (links | edit)
- Sex-determining region Y protein (links | edit)
- Rubinstein–Taybi syndrome (links | edit)
- Zinc finger inhibitor (links | edit)
- Estrogen receptor (links | edit)
- Fuchs' dystrophy (links | edit)
- FOXP3 (links | edit)
- General transcription factor (links | edit)
- ParaHox (links | edit)
- HMGN (links | edit)
- Saethre–Chotzen syndrome (links | edit)
- E2F (links | edit)
- Progesterone receptor (links | edit)
- Androgen receptor (links | edit)
- Sex hormone receptor (links | edit)
- Hepatocyte nuclear factor 4 (links | edit)
- Spinal and bulbar muscular atrophy (links | edit)
- NF-κB (links | edit)
- Hypoxia-inducible factor (links | edit)