(Q40442368)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

review article

1 reference

reason for preferred rank

title

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

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

11 June 2024

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

1 reference

chromosomal deletion syndrome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

author name string

J. C. Marinoni

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

R. E. Stevenson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

J. P. Evans

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

D. Geshuri

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

M. C. Phelan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

C. E. Schwartz

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7606850

11 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7606850

11 June 2024

publication date

1 February 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

21 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1995.tb03930.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-0004.1995.tb03930.x

11 June 2024

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

11 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

47

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

2

1 reference

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21 October 2019

page(s)

90-95

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization

21 October 2019

cites work

5

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

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

11 June 2024

6

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

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

11 June 2024

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.

11 June 2024

11

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

Ectrodactyly and proximal/intermediate interstitial deletion 7q

11 June 2024

12

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

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

11 June 2024

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

Inverted insertion of chromosome 7q and ectrodactyly

11 June 2024

15

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

A routine method for the establishment of permanent growing lymphoblastoid cell lines

11 June 2024

16

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

Deletion of 7q22 and ectrodactyly

11 June 2024

19

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

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

11 June 2024

20

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

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

11 June 2024

25

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

11 June 2024

27

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

A second-generation linkage map of the human genome

11 June 2024

30

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03930.X

11 June 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7606850%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference