Wikidata

(Q28284655)

English

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

scientific article

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title
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 (English)
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author name string
N H Robin
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1
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G J Feldman
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2
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A L Aronson
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3
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H F Mitchell
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4
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R Weksberg
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5
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C O Leonard
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6
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B K Burton
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7
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K D Josephson
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8
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R Laxová
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9
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K A Aleck
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10
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J E Allanson
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11
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M L Guion-Almeida
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12
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R A Martin
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13
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L G Leichtman
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14
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R A Price
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15
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M Muenke
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17
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publication date
December 1995
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volume
11
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page(s)
459-61
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issue
4
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cites work

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