Incidental detection of a de novo 16p13.3 microdeletion encompassing PKD1 and a familial Yq11.223 microdeletion encompassing DAZ1 in a fetus with encephalocele on prenatal ultrasound and amniotic band syndrome

Author:

Chen Chih-Ping

Funder

National Science and Technology Council

Publisher

Elsevier BV

Reference10 articles.

1. First-trimester sonographic demonstration of a mobile cranial cyst associated with anencephaly and amniotic band sequence;Chen;Ultrasound Obstet Gynecol,2001

2. Prenatal diagnosis of limb-body wall complex with craniofacial defects, amniotic bands, adhesions and upper limb deficiency;Chen;Prenat Diagn,2001

3. Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies;Chen;Genet Counsel,2007

4. Syndromes, disorders and maternal risk factors associated with neural tube defects (III);Chen;Taiwan J Obstet Gynecol,2008

5. Prenatal diagnosis of acrania associated with facial defects, amniotic bands and limb-body wall complex;Chen;Ultrasound Obstet Gynecol,2002

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