(Q33675025)

28 July 2017

1 reference

title

Cleft hand/foot: clinical and developmental aspects (English)

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28 July 2017

Buss PW

1

1 reference

28 July 2017

language of work or name

English

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publication date

1 September 1994

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

31

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28 July 2017

issue

9

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28 July 2017

page(s)

726-730

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CRANIO-FACIAL DYSOSTOSIS AND MALFORMATIONS OF FEET.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

An epidemiological study of isolated split hand/foot in Hungary, 1975-1984.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Sonic hedgehog mediates the polarizing activity of the ZPA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Syndactylies and polydactylies: embryological overview and suggested classification

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Tetraectrodactyly and other skeletal manifestations in the fetal alcohol syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Congenital ectodermal dysplasia with hearing loss.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Dominant ectrodactyly and possible germinal mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Newly recognized ectrodactyly/deafness syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Limb reduction defects in over one million consecutive livebirths

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Limb reduction defects in humans associated with prenatal isotretinoin exposure

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

The apical ectodermal ridge regulates Hox-7 and Hox-8 gene expression in developing chick limb buds

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Position-dependent expression of two related homeobox genes in developing vertebrate limbs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Expression of the homeobox Hox-4 genes and the specification of position in chick wing development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Retinoids and their targets in vertebrate development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Retinoic acid, local cell-cell interactions, and pattern formation in vertebrate limbs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Constrictive bands in the human

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Mechanisms of limb development and malformation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

A gene complex controlling segmentation in Drosophila

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Congenital central hand deficit

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050086

Ectrodactyly--evidence in favour of a disturbed segregation in the offspring of affected males

30 October 2018

1 reference

12 December 2020

Split-hand and split-foot deformity inherited as an autosomal recessive trait

1 reference

12 December 2020

A problem for genetic counselling - split hand deformity

1 reference

12 December 2020

Dactylaplasia in mice a two-locus model for development anomalies

1 reference

12 December 2020

[Interstitial deletion of the long arm of chromosome 7 and its clinical correlations]

1 reference

12 December 2020

Limb reduction deformities in child exposed to isotretinoin in utero on gestation days 26-40 only

1 reference

12 December 2020

Autosomal dominant ectrodactyly and absence of long bones of upper or lower limbs: further clinical delineation

1 reference

12 December 2020

Coordinate expression of the murine Hox-5 complex homoeobox-containing genes during limb pattern formation

1 reference

12 December 2020

A tool for transgenesis

1 reference

12 December 2020

EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3

1 reference

12 December 2020

Inverted insertion of chromosome 7q and ectrodactyly

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.31.9.726

1 reference

28 July 2017

1 reference

28 July 2017

1 reference