Preaxial polydactyly in an individual with Wiedemann-Steiner syndrome caused by a novel nonsense mutation in KMT2A (vol 173A, pg 821, 2017)

被引：0
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作者：
Enokizono, T.
Ohto, T.
Tanaka, R.
Tanaka, M.
Suzuki, H.
Sakai, A.
Imagawa, K.
Fukushima, H.
Iwabuti, A.
Fukushima, T.
Sumazaki, R.
Uehara, T.
Takenouchi, T.
Kosaki, K.
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2020年 / 182卷 / 09期
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D O I：
10.1002/ajmg.a.61774
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
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页码：2195 / 2195
页数：1
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