[HTML][HTML] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider… - Journal of human …, 2006 - nature.com
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider… - Journal of Human …, 2006 - infona.pl
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
[引用][C] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
C MS - J Hum Genet, 2006 - cir.nii.ac.jp
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with
associated dental anomalies in Pakistani families | CiNii Research CiNii 国立情報学研究所 学術 …
associated dental anomalies in Pakistani families | CiNii Research CiNii 国立情報学研究所 学術 …
[PDF][PDF] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider, W Ahmad - J Hum Genet, 2006 - researchgate.net
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
[PDF][PDF] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider, W Ahmad - J Hum Genet, 2006 - academia.edu
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.
MS Chishti, D Muhammad, M Haider… - Journal of Human …, 2006 - europepmc.org
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, M Dost, H Mahmud… - Journal of Human …, 2006 - search.proquest.com
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad… - Journal of human …, 2006 - pubmed.ncbi.nlm.nih.gov
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.
MS Chishti, D Muhammad, M Haider… - Journal of Human …, 2006 - search.ebscohost.com
Tooth agenesis constitutes the most common anomaly of dental development in humans. In
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
the majority of familial cases of hypodontia alone or in association with other anomalies, the …
[引用][C] A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
MS Chishti, D Muhammad, M Haider - Journal of human genetics/Japan …, 2006 - cir.nii.ac.jp
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with
associated dental anomalies in Pakistani families | CiNii Research CiNii 国立情報学研究所 学術 …
associated dental anomalies in Pakistani families | CiNii Research CiNii 国立情報学研究所 学術 …