A second family with blepharo-naso-facial syndrome-Reference-Cited by-同舟云学术

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A second family with blepharo-naso-facial syndrome

Published:2002-07 Issue:3 Volume:11 Page:191-194
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

Allanson Judith E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference5 articles.

1. Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome

2. Eye Findings in the Blepharo-Naso-Facial Malformation Syndrome

3. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness

4. Nablus mask-like facial syndrome

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1. Nablus mask‐like facial syndrome: Report of an atypical case with 8q21.3–q22.1 deletion;American Journal of Medical Genetics Part A;2024-07-22

2. Atlantoaxial dislocation in the setting of NMLFS;European Journal of Medical Genetics;2024-06

3. Intraoral findings of a patient with Nablus mask-like facial syndrome and dental treatment approaches: a case report and literature review;Journal of Clinical Pediatric Dentistry;2023

4. Nablus syndrome: Easy to diagnose yet difficult to solve;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-12

5. A newborn diagnosed with van Maldergem syndrome;Clinical Dysmorphology;2018-04

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