Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution.

Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution.

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http://www.wikidata.org/entity/Q38204785
Heterotaxy Polysplenia Syndrome In An Adult With Unique Vascular Anomalies: Case Report With Review Of LiteratureA case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder.Asplenia in children with congenital heart disease as a cause of poor outcome.A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle.Human B-cell memory is shaped by age- and tissue-specific T-independent and GC-dependent events.Prevalence of Noncardiac and Genetic Abnormalities in Neonates Undergoing Cardiac Operations: Analysis of The Society of Thoracic Surgeons Congenital Heart Surgery Database.Left Upper-Quadrant Appendicitis in a Patient with Congenital Intestinal Malrotation and Polysplenia., a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in
P2860

Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution.

Item
http://www.wikidata.org/entity/Q38204785
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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Defects in laterality with emp ...... eries at a single institution.
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type
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Defects in laterality with emp ...... eries at a single institution.
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Defects in laterality with emp ...... eries at a single institution.
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P1433
P1476
P2093
P2860
P304
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P356
P433
P478
P50
P577
P698
P921
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P1433
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Defects in laterality with emp ...... eries at a single institution.
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P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P921