(Q34460910)

2 August 2017

title

Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation (English)

1 reference

2 August 2017

6

Hiroki Kurahashi

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2 August 2017

Hiroki Kano

1

1 reference

2 August 2017

Kenji Kurosawa

2

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2 August 2017

Emiko Horii

3

1 reference

2 August 2017

Shiro Ikegawa

4

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2 August 2017

Hideki Yoshikawa

5

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2 August 2017

Tatsushi Toda

7

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2 August 2017

publication date

19 October 2005

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2 August 2017

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2 August 2017

volume

118

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2 August 2017

issue

3-4

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2 August 2017

page(s)

477-483

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Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

2 August 2017

cites work

1 reference

12 December 2020

Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac

1 reference

12 December 2020

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

1 reference

12 December 2020

A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.

1 reference

12 December 2020

Ectro-amelia syndrome associated with an interstitial deletion of 7q.

1 reference

12 December 2020

X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred.

1 reference

12 December 2020

Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25

1 reference

12 December 2020

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant

1 reference

12 December 2020

Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review

1 reference

12 December 2020

A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.

1 reference

12 December 2020

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

1 reference

12 December 2020

Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

1 reference

12 December 2020

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24

1 reference

12 December 2020

A split hand-split foot (SHFM3) gene is located at 10q24-->25.

1 reference

12 December 2020

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly

1 reference

12 December 2020

Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2‐q22.1

1 reference

12 December 2020

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

1 reference

12 December 2020

Dactylaplasia in mice a two-locus model for development anomalies

1 reference

12 December 2020

Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

1 reference

12 December 2020

Ectrodactyly and proximal/intermediate interstitial deletion 7q

1 reference

12 December 2020

Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.

1 reference

12 December 2020

Bilateral split hand/foot malformation and inv(7)(p22q21.3)

1 reference

12 December 2020

10.1007/S00439-005-0074-0

Identifiers

DOI

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Dimensions Publication ID

2 August 2017

1008637917

0 references

1 reference