𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families

✍ Scribed by Li, Jun ;Tabor, Holly K. ;Nguyen, Loan ;Gleason, Christopher ;Lotspeich, Linda J. ;Spiker, Donna ;Risch, Neil ;Myers, Richard M.


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
107 KB
Volume
114
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


No association between allelic variants
✍ Gallagher, Louise ;Hawi, Ziarih ;Kearney, Geraldine ;Fitzgerald, Michael ;Gill, πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 64 KB πŸ‘ 1 views

## Abstract Two recent studies have reported conflicting findings of association of a variant in the __HOXA1__ gene and autism. To try to resolve the conflict in findings, we conducted an association study in 78 Irish families of the reported DNA variants. We did not find statistically significant

Lack of expansion of triplet repeats in
✍ Holden, Jeanette J. A.; Wing, Maggie; Chalifoux, Maryse; Julien-Inalsingh, Colin πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 498 KB πŸ‘ 1 views

Sib, twin, and family studies have shown that a genetic cause exists in many cases of autism, with a portion of cases associated with a fragile X chromosome. Three folatesensitive fragile sites in the Xq27+Xq28 region have been cloned and found to have polymorphic trinucleotide repeats at the respec

Lack of association between serotonin tr
✍ Persico, Antonio M.; Militerni, Roberto; Bravaccio, Carmela; Schneider, Cindy; M πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 30 KB πŸ‘ 2 views

The present study was designed to assess linkage and linkage disequilibrium in two new ethnically distinct samples of families with primary autistic probands. The 5-HTT promoter repeat was genotyped in 54 singleton families collected in Italy and in 32 singleton and 5 multiplex families collected in

Lack of association between temporal lob
✍ Buono, R.J.; Ferraro, T.N.; O'Connor, M.J.; Sperling, M.R.; Abbey, M.; Finanger, πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 12 KB πŸ‘ 1 views

Genetic linkage studies in rodents and humans have identified specific chromosomal regions harboring seizure susceptibility genes. We have identified a novel polymorphism in the human alpha 2 subunit gene (ATP1A2) of the sodium potassium transporting ATPase (NaK-pump), a candidate gene for human tem