Browsing by Author Niikawa N.

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Showing results 1 to 4 of 4
Issue DateTitleAuthor(s)
2002A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai familyKantaputra P.N.; Yamasaki K.; Ishida T.; Kishino T.; Niikawa N.
2009Mapping human genetic diversity in AsiaAbdulla M.A.; Ahmed I.; Assawamakin A.; Bhak J.; Brahmachari S.K.; Calacal G.C.; Chaurasia A.; Chen C.-H.; Chen J.; Chen Y.-T.; Chu J.; Cutiongco-de La Paz E.M.C.; De Ungria M.C.A.; Delfin F.C.; Edo J.; Fuchareon S.; Ghang H.; Gojobori T.; Han J.; Ho S.-F.; Hoh B.P.; Huang W.; Inoko H.; Jha P.; Jinam T.A.; Jin L.; Jung J.; Kangwanpong D.; Kampuansai J.; Kennedy G.C.; Khurana P.; Kim H.-L.; Kim K.; Kim S.; Kim W.-Y.; Kimm K.; Kimura R.; Koike T.; Kulawonganunchai S.; Kumar V.; Lai P.S.; Lee J.-Y.; Lee S.; Liu E.T.; Majumder P.P.; Mandapati K.K.; Marzuki S.; Mitchell W.; Mukerji M.; Naritomi K.; Ngamphiw C.; Niikawa N.; Nishida N.; Oh B.; Oh S.; Ohashi J.; Oka A.; Ong R.; Padilla C.D.; Palittapongarnpim P.; Perdigon H.B.; Phipps M.E.; Png E.; Sakaki Y.; Salvador J.M.; Sandraling Y.; Scaria V.; Seielstad M.; Sidek M.R.; Sinha A.; Srikummool M.; Sudoyo H.; Sugano S.; Suryadi H.; Suzuki Y.; Tabbada K.A.; Tan A.; Tokunaga K.; Tongsima S.; Villamor L.P.; Wang E.; Wang Y.; Wang H.; Wu J.-Y.; Xiao H.; Xu S.; Yang J.O.; Shugart Y.Y.; Yoo H.-S.; Yuan W.; Zhao G.; Zilfalil B.A.
2002A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feetKondoh S.; Sugawara H.; Harada N.; Matsumoto N.; Ohashi H.; Sato M.; Kantaputra P.N.; Ogino T.; Tomita H.; Ohta T.; Kishino T.; Fukushima Y.; Niikawa N.; Yoshiura K.-I.
2002A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: A new distal symphalangism syndrome?Kantaputra P.N.; Kinoshita A.; Limwonges C.; Praditsup O.; Niikawa N.