Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report.

Haggerty, Abigail; Spaulding, Joanna; Fisher, Sara; Byers, Benjamin; Mahoney, Nicolle; Nelson, Marilu; Althof, Pamela; Dave, Bhavana

Haggerty, Abigail; Spaulding, Joanna; Fisher, Sara; Byers, Benjamin; Mahoney, Nicolle; Nelson, Marilu; Althof, Pamela; Dave, Bhavana.

Afiliação

Haggerty A; Warren G. Sanger Human Genetics Laboratory, University of Nebraska Medical Center/Nebraska Medicine, Omaha, Nebraska, USA, abhaggerty@nebraskamed.com.
Spaulding J; Warren G. Sanger Human Genetics Laboratory, University of Nebraska Medical Center/Nebraska Medicine, Omaha, Nebraska, USA.
Fisher S; Department of Genetic Medicine, Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Byers B; Department of Medical Sciences, College of Allied Health Professions, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Mahoney N; Department of Obstetrics and Gynecology, Bryan Health, Lincoln, Nebraska, USA.
Nelson M; Gynecology & Fertility, Gynecology & Fertility P.C., Lincoln, Nebraska, USA.
Althof P; Warren G. Sanger Human Genetics Laboratory, University of Nebraska Medical Center/Nebraska Medicine, Omaha, Nebraska, USA.
Dave B; Warren G. Sanger Human Genetics Laboratory, University of Nebraska Medical Center/Nebraska Medicine, Omaha, Nebraska, USA.

Cytogenet Genome Res ; 162(11-12): 609-616, 2022.

Article em En | MEDLINE | ID: mdl-36787703

Palavras-chave

Cytogenetics; Derivative chromosome; FISH; Mosaicism; Reproductive risk; SNP microarray

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Cytogenet Genome Res Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article

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