(Q42661519)

4 November 2017

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

1 reference

4 November 2017

Cobben JM

1 reference

4 November 2017

Verheij JB

1 reference

4 November 2017

Eisma WH

1 reference

4 November 2017

Robinson PH

1 reference

4 November 2017

Zwierstra RP

1 reference

4 November 2017

Leegte B

1 reference

4 November 2017

Castedo S

1 reference

4 November 2017

language of work or name

English

0 references

publication date

1 May 1995

1 reference

Journal of Medical Genetics

4 November 2017

1 reference

4 November 2017

1 reference

4 November 2017

1 reference

4 November 2017

375-378

1 reference

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

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Non-Mendelian transmission in a human developmental disorder: split hand/split foot

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Vascular abnormalities at the site of limb deficiency

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050433

Deletion of 7q22 and ectrodactyly

27 May 2018

1 reference

12 December 2020

EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations

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

The effect of Robertsonian translocation on recombination on chromosome 21

1 reference

12 December 2020

Human situs determination and chromosome constitution 46,XY,ins(7;8)(q22;q12q24)

1 reference

12 December 2020

EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3)

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.32.5.375

1 reference

4 November 2017

1 reference

4 November 2017

PubMed publication ID

7616545

1 reference