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A complex bilateral polysyndactyly disease locus maps to chromosome 7q36
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instance of
scholarly article
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title
A complex bilateral polysyndactyly disease locus maps to chromosome 7q36
(English)
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main subject
polysyndactyly
1 reference
based on heuristic
inferred from title
author name string
O Tsukurov
series ordinal
1
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A Boehmer
series ordinal
2
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J Flynn
series ordinal
3
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J P Nicolai
series ordinal
4
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B C Hamel
series ordinal
5
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S Traill
series ordinal
6
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D Zaleske
series ordinal
7
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H J Mankin
series ordinal
8
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H Yeon
series ordinal
9
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C Ho
series ordinal
10
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language of work or name
English
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publication date
March 1994
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published in
Nature Genetics
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volume
6
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issue
3
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page(s)
282-6
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cites work
Polydactyly in the Bible
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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inferred from DOI database lookup
The study of genetic variation in Nigeria. II. The genetics of polydactyly
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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inferred from DOI database lookup
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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A second-generation linkage map of the human genome
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https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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Isolation and chromosomal localization of the human En-2 gene
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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Mapping of the two mouse engrailed-like genes: close linkage of En-1 to dominant hemimelia (Dh) on chromosome 1 and of En-2 to hemimelic extra-toes (Hx) on chromosome 5.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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Closure of a genetic linkage map of human chromosome 7q with centromere and telomere polymorphisms
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0394-282
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7 January 2021
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Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndrome
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7 January 2021
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Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).
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https://api.crossref.org/works/10.1038%2FNG0394-282
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7 January 2021
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Engrailed: a gene controlling compartment and segment formation in Drosophila
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7 January 2021
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Homeobox genes and axial patterning
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7 January 2021
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Targeted misexpression of Hox-4.6 in the avian limb bud causes apparent homeotic transformations
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https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0394-282
retrieved
7 January 2021
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Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines
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https://api.crossref.org/works/10.1038%2FNG0394-282
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7 January 2021
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Identifiers
DOI
10.1038/NG0394-282
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PubMed publication ID
8012391
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