Brachytelephalangic Chondrodysplasia Punctata: Prenatal Diagnosis and Postnatal Outcome-Reference-Cited by-同舟云学术

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Brachytelephalangic Chondrodysplasia Punctata: Prenatal Diagnosis and Postnatal Outcome

Published:2010 Issue:3 Volume:28 Page:186-190
ISSN:1421-9964
Container-title:Fetal Diagnosis and Therapy
language:en
Short-container-title:Fetal Diagn Ther

Author:

Boulet S.,Dieterich K.,Althuser M.,Nugues F.,Durand C.,Charra C.,Schaal J.P.,Jouk P.S.

Publisher

S. Karger AG

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Obstetrics and neonatal outcomes of binder phenotype with antenatal diagnosis: A case report and literature review;Journal of Gynecology Obstetrics and Human Reproduction;2024-12

2. Rare Association of Fetal Chondrodysplasia Punctata in Maternal SLE: A Case Report;Journal of Fetal Medicine;2021-04-02

3. The complementary role of imaging modalities in Binder phenotype. Can prognostic factors of neonatal respiratory distress be found?;Prenatal Diagnosis;2019-05-10

4. Binder syndrome: a phenotype rather than a definitive diagnosis?;Ultrasound in Obstetrics & Gynecology;2019-01

5. Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata;Pediatric Radiology;2018-03-23

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