“Minimal” holoprosencephaly in a 14q deletion syndrome patient-Reference-Cited by-同舟云学术

“Minimal” holoprosencephaly in a 14q deletion syndrome patient

Published:2017-11-14 Issue:12 Volume:173 Page:3216-3220
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Della Giustina Elvio¹^ORCID,Iodice Alessandro¹,Spagnoli Carlotta¹,Giovannini Simona²,Frattini Daniele¹,Fusco Carlo¹,Gobbi Giuseppe²,Zollino Marcella³,Neri Giovanni³^ORCID

Affiliation:

1. Child Neurology Unit; IRCCS; Santa Maria Nuova Hospital; Reggio Emilia Italy

2. Child Neurology Unit; Bellaria Hospital; IRCCS Institute of Neurological Sciences; Bologna Italy

3. Institute of Medical Genetics; Catholic University School of Medicine; Rome Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

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2. Middle interhemispheric fusion: An unusual variant of holopeosencephaly;Barkovich;American Journal of Neuroradiology,1993

3. Prenatal diagnosis of the novo proximal interstitial deletion of 14q associated with cebocephaly;Chen;Journal of Medical Genetics,1997

4. Ocular manifestations of chromosome 14 terminal deletion;Chung;Journal of Pediatric Ophthalmology and Strabismus,2006

5. Septopreoptic holoprosencephaly: A mild subtype associated with midline craniofacial anomalies;Hahn;American Journal of Neuroradiology,2010

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1. Midline Brain Anomalies II: Holoprosencephaly;MR Imaging of the Fetus;2022

2. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26