Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region
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Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review.Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization.Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.
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Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region
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article
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im Oktober 2008 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в жовтні 2008
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name
Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
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Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
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type
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Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
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Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
@nl
prefLabel
Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
@en
Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
@nl
P2093
P50
P356
P1476
Familial deletion 11q14.3-q22. ...... haplosufficient 8.5 Mb region
@en
P2093
A Tchirkov
C Francannet
M Giollant
T Roucaute
P304
P356
10.1002/AJMG.A.32511
P407
P577
2008-10-01T00:00:00Z