Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

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作者： Wafa,Slimani ^[1] ; Hela,Ben Khelifa ^[1] ; Sarra,Dimassi ^[1] ; Fatma-Zohra,Chioukh ^[2] ; Afef,Jelloul ^[1] ; Molka,Kammoun ^[1] ; Hanene,Hannachi ^[1] ; Sarra,Bouslah ^[3] ; Nesrine,Jammali ^[4] ; Damien,Sanlaville ^[5] ; Ali,Saad ^[1] ; Soumaya,Mougou-Zerelli ^[6]

作者单位： 1Laboratory of Human cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia. ^[1] Neonatology Department, Hospital of Fattouma Bourguiba, Monastir, Tunisia. ^[2] 3Pediatric department, Farhat Hached University Hospital, Sousse, Tunisia. ^[3] 4Department of Child psychiatry, Fattouma Bourguiba Hospital, Monastir, Tunisia. ^[4] 5Centre de Biologie et Pathologie Est, CHU de Lyon HCL, Lyon, France. ^[5] 6Université de Sousse, Faculté de Médecine de Sousse, Hopital Farhat Hached, UR035P2, 4000 Sousse, Tunisia. ^[6]

关键词 Array CGH FISH Small supernumerary chromosome marker Tetrasomy 18p

DOI 10.1186/s13039-019-0414-8

PMID 30774715

发布时间 2024-07-14

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Molecular cytogenetics

2019年12卷

5页

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Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Molecular cytogenetics

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Molecular cytogenetics

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Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Molecular cytogenetics

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Molecular cytogenetics

相关期刊

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