HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

Esther Vamos Selected Research

Sabinas brittle hair syndrome

3/2005Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!


Choose Username:
Email:
Password:
Verify Password:


Esther Vamos Research Topics

Disease

1Brain Diseases (Brain Disorder)
01/2006
1Mental Retardation (Idiocy)
03/2005

Drug/Important Bio-Agent (IBA)

1Phosphotransferases (Kinase)IBA
01/2006
1Sabinas brittle hair syndromeIBA
03/2005
1Trichorrhexis nodosa syndromeIBA
03/2005