Turner's syndrome in fetal life

Surerus, E., Huggon, I. C., Allan, L. D.·2003·Ultrasound in Obstetrics & Gynecology

Cited by (106)

Items 101–106 of 106

  1. Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort
    Akanksha M Tiwari, Kavyashree Padumale, Apoorva Bhandaru, Sushma Gandla, Suparna Maji, Ram Kumar, Honey Sharma, Nithyanandan Thangavel, Sameer Phalke, N Faheena et al. · 2025 · medRxiv
  2. Óbito fetal em gestações únicas com diagnóstico de trissomias dos cromossomos 21,18 13 e monossomia do X
    Vanessa Vigna Goulart · 2014
  3. New insight about early miscarriage: a prenatal data-based study
    Yuanhang Zhu, Yaming Liu, Chunying Ren, Jing Liu, Qian Yang, Naiqi Li, Ting Wang, Ping Zhang, Jing Xue, Chenchen Ren et al. · 2026 · Journal of Translational Medicine
  4. Fetal pathology meets clinical genetics – on the value of a comprehensive postmortem examination
    Susanne Sprung, BSc Martina Messner, Renate Lunzer, Irene Mutz‐Dehbalaie, Patricia Döttelmayer, Karin Freund‐Unsinn, Christine Fauth · 2026 · Medizinische Genetik
  5. Growth hormone therapy in Turner syndrome: Do cytogenetic subtypes influence outcomes?
    Ingrid-Ioana Herșcovici, Monica-Cristina Pânzaru, Georgiana Constantinescu, Letiția Leuștean, Maria-Christina Ungureanu, Cristina Preda, Cristina Rusu · 2026 · Endocrinología Diabetes y Nutrición
  6. Growth hormone therapy in Turner syndrome: Do cytogenetic subtypes influence outcomes?
    Ingrid-Ioana Herșcovici, Monica-Cristina Pânzaru, Georgiana Andreea Constantinescu, Letiția Leuștean, Maria-Christina Ungureanu, Cristina Preda, Cristina Rusu · 2026 · Endocrinología Diabetes y Nutrición (English ed )