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SHFM2 gene
Known as:
SHFM2
, SHSF2
, split hand/foot malformation (ectrodactyly) type 2
National Institutes of Health
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2 relations
SHFM1 gene
SPLIT-HAND/FOOT MALFORMATION 2
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Mise au point sur la pathogenèse des fentes médianes de la main
S. Guero
,
M. Holder-Espinasse
Hand Surgery and Rehabilitation
2018
Corpus ID: 86677687
2015
2015
Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization.
Chin-Jui Wu
,
Yidi Su
,
T. Lin
,
L. Tseng
,
Kuang‐Han Chao
Taiwanese Journal of Obstetrics & Gynecology
2015
Corpus ID: 3008338
2006
2006
[A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
Wei Yang
,
Zhou-jun Hu
,
+9 authors
Xue Zhang
Zhonghua yi xue za zhi
2006
Corpus ID: 25618238
OBJECTIVE To identify the disease-causing genetic alteration of split-hand/split-foot malformation (SHFM) in a Chinese family…
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Highly Cited
1995
Highly Cited
1995
A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.
M. Nuñes
,
G. Schutt
,
+4 authors
J. Evans
Human Molecular Genetics
1995
Corpus ID: 42472471
Ectrodactyly (split hand/split foot malformation, SHSF) is a human limb malformation characterized by absent central digital rays…
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