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Opening Pandora's box: abnormal genetic carrier screening and need for lifetime follow-up.
Strauss, Tirtza Spiegel; Boniferro, Emily; Brockhoff, Erika; Johnson, Anna; Schneider, Emily; Grubman, Olivia; Cole, David; Hussain, Farrah; Ashmead, Graham; Al-Ibraheemi, Zainab; Brustman, Lois.
Affiliation
  • Strauss TS; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019. Electronic address: tirtza.strauss@mountsinai.org.
  • Boniferro E; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Brockhoff E; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Johnson A; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Schneider E; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Grubman O; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Cole D; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Hussain F; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Ashmead G; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Al-Ibraheemi Z; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
  • Brustman L; Division of Maternal Fetal Medicine, Mount Sinai West, Icahn School of Medicine at Mount Sinai, 1000 10th Ave., New York, NY 10019.
Am J Obstet Gynecol MFM ; 5(3): 100820, 2023 03.
Article in En | MEDLINE | ID: mdl-36455867
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bernard-Soulier Syndrome / Muscular Dystrophy, Duchenne / Nijmegen Breakage Syndrome / Factor XI Deficiency Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Pregnancy Language: En Journal: Am J Obstet Gynecol MFM Year: 2023 Document type: Article
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bernard-Soulier Syndrome / Muscular Dystrophy, Duchenne / Nijmegen Breakage Syndrome / Factor XI Deficiency Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Pregnancy Language: En Journal: Am J Obstet Gynecol MFM Year: 2023 Document type: Article