Longitudinal observation of a patient with Rieger syndrome and interstitial deletion 4 (q25-q31.1)-Reference-Cited by-同舟云学术

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Longitudinal observation of a patient with Rieger syndrome and interstitial deletion 4 (q25-q31.1)

Published:2010-04 Issue:4 Volume:152A Page:977-981
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Moreira Lilia,Schinzel Albert,Baumer Alessandra,Pinto Paula,Góes Fátima,Falcão Maria de Lourdes,Barbosa Ana Luiza,Riegel Mariluce

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Rieger syndrome: A clinical, molecular, and biochemical analysis;Amendt;Cell Mol Life Sci,2000

2. A new case of an interstitial deletion (4)(q25q27) characterized by molecular cytogenetic techniques and review of the literature;Becker;Eur J Pediatr,2003

3. Autosomal dominant iridodysgenesis with associated somatic anomalies: Four-generation family with Rieger's syndrome;Chisholm;Br J Ophthalmol,1983

4. Rieger syndrome and interstitial 4q26 deletion;Fryns;Genet Couns,1992

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1. 4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay;Case Reports in Genetics;2023-02-09

2. A review of wombat diet and nutrition;Australian Mammalogy;2021

3. Renal Dysplasia and Progressive Renal Failure in a Newborn with Interstitial Chromosome 4 Deletion 4q25-28.3: A New Phenotype?;Journal of Pediatric Genetics;2020-01-22

4. 4q25 microdeletion encompassing PITX2 : A patient presenting with tetralogy of Fallot and dental anomalies without ocular features;European Journal of Medical Genetics;2018-02

5. Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome;Acta Ophthalmologica;2016-03-24

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