FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

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Murine model indicates 22q11.2 signaling adaptor CRKL is a dosage-sensitive regulator of genitourinary development.Transcriptome analysis of Xenopus orofacial tissues deficient in retinoic acid receptor function

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FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

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2010 nî lūn-bûn

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2010年の論文

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FOXD1 Duplication Causes Branc ...... using Eye Effects in Zebrafish

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FOXD1 Duplication Causes Branc ...... sing Eye Effects in Zebrafish.

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FOXD1 Duplication Causes Branc ...... using Eye Effects in Zebrafish

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FOXD1 Duplication Causes Branc ...... sing Eye Effects in Zebrafish.

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FOXD1 Duplication Causes Branc ...... using Eye Effects in Zebrafish

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FOXD1 Duplication Causes Branc ...... sing Eye Effects in Zebrafish.

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P1476

FOXD1 Duplication Causes Branc ...... using Eye Effects in Zebrafish

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I Balikova

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J R Vermeesch

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J-P Fryns

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K Devriendt

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P2860

Characterization of ANKRA, a novel ankyrin repeat protein that interacts with the cytoplasmic domain of megalin

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

A protein complex required for signal-sequence-specific sorting and translocation

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

TFAP2A mutations result in branchio-oculo-facial syndrome

Identification of a novel, putative Rho-specific GDP/GTP exchange factor and a RhoA-binding protein: control of neuronal morphology

Stages of embryonic development of the zebrafish

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

AP-2alpha knockout mice exhibit optic cup patterning defects and failure of optic stalk morphogenesis

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scholarly article

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10.1159/000327707

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22140378

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Danio rerio

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FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

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P2860

P2860

FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

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