Gene mapping of developmental dysplasia of the hip in chromosome 17q21 region / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 620-625, 2010.
Article
Dans Zh
| WPRIM
| ID: wpr-234351
Responsable en Bibliothèque :
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To map the susceptibility gene of developmental dysplasia of the hip(DDH) in chromosome 17q21 region.</p><p><b>METHODS</b>According to the number of alleles (≥ 5), heterozygosity (≥ 0.70) and polymorphic information content (PIC≥ 0.5), 11 STR markers in the 17q21 region were chosen for transmission disequilibrium test (TDT). STR markers were amplified by PCR and genotypes were analyzed by capillary electrophoresis in 103 trio families. TDT was used to locate the susceptibility gene in 17q21 region.</p><p><b>RESULTS</b>Because of a low genetic polymorphism, D17S810 and D17S931 loci were removed from the TDT. Transmission disequilibrium was detected at D17S855, D17S858, D17S806, D17S1877, D17S941, D17S752 and D17S790, which overlapped 11.7 cM in 17q21. However, no transmission disequilibrium was found at D17S1787 and D17S787. Thus, the susceptibility gene for DDH was located in the chromosome region between D17S855 and D17S790.</p><p><b>CONCLUSION</b>The susceptibility gene for DDH is narrowed to an 11.7 cM region of 17q21.31-17q22, between STR loci D17S855 and D17S790.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Polymorphisme génétique
/
Chromosomes humains de la paire 17
/
Déséquilibre de liaison
/
Cartographie chromosomique
/
Clonage moléculaire
/
Répétitions microsatellites
/
Prédisposition génétique à une maladie
/
Génétique
/
Luxation congénitale de la hanche
/
Méthodes
Limites du sujet:
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
langue:
Zh
Texte intégral:
Chinese Journal of Medical Genetics
Année:
2010
Type:
Article