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BETA THALASEMIA MUTATION DETECTION (NAGERCOIL KANIYAKUMARI DISTRICT)

BETA THALASEMIA MUTATION DETECTION (IVS1-5G-C,619 BP DELETION , cd 8/9 +G, IVS1-1G-T, 41/42-TTCT LAUNCHING IN INDIA

WE ARE PRIVILLEGED TO ANNOUCED THE LAUNCHING OF THE ABOVE SAID TEST IN INDIA.,

THE PROCEDURE
MULTIPLEX PCR.

CONTIANER TYPE
AMINOTIC FLUID/CVS IN STERILE TISSUES CULTURE MEDIA OR SALINE / FETAL BLOOD IN EDTA+EDTA WHOLE BLOOD FOR BOTH

REPORT TIME
8DAYS FROM THE DATE OF RECEIPT OF THE SAMPLE TO OUR LAB.

PRICES
SHALL INFORM WHEN YOU CONTACT US .


INTRODUCTION
The most common inherited diseases in humans result from mutations in the beta-globin gene com-plex and the alpha-globin gene complex. We refer
to the beta-globin gene complex as HBBC, com-posed of the genes HBE1 (MIM# 142100), HBG2(MIM# 142250), HBG1(MIM# 142200), HBD(MIM# 42000), and HBB MIM# 141900),which encode the epsilon-, gamma-, Agamma-,delta-, and beta-globin polypeptides, respectively.We refer to the lpha-globin gene complex asHBAC, composed of the genes HBZ2 (MIM#142310), HBA2(MIM# 141850), HBA1(MIM#141800), and HBQ1 (MIM# 42240), which en-code the zeta-, alpha2-, alpha1-, and possibly theta-globin olypeptides, respectively.

FOR MORE DETAILS PLEASE CONTACT US AT

Advanced Technologies Inc,
1St Floor Smm Bldg, Next To Canara Bank,
K. P. Road, Nagercoil – 629 001
Kaniyakumari Dist, Tamil Nadu, India.
Mob: 9360036111,




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