Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Prenatal diagnosis of congenital upper limb differences: a current concept review.

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Q38997472-71484F60-1301-4A34-B976-EBD4DDD447DC

P2860

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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P1476

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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P2093

Ambika Srikanth

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Aswini Sivasankaran

http://www.w3.org/2001/XMLSchema#string

Chandra R Samuel

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Deenadayalu Anuradha

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Jayarama S Kadandale

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Pooja S Kulshreshtha

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P2860

Receptor complexes for each of the Class 3 Semaphorins

Rnf165/Ark2C enhances BMP-Smad signaling to mediate motor axon extension

Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.

Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

Semaphorin 3E-Plexin-D1 signaling controls pathway-specific synapse formation in the striatum

Mouse model of split hand/foot malformation type I

The role of the Rho GTPases in neuronal development

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287-296

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scholarly article

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10.1159/000443708

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2016-02-03T00:00:00Z

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27022330

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4802982

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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P2860

P2860

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

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P1433

P1476

P2093

P2860

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P356

P433

P478

P577

P698

P932

P356

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P1476

P2093

P2860

P304

P31

P356

P433

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P577

P698

P932