Cat eye syndrome and growth hormone deficiency with pituitary anomalies: A case report and review of the literature
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference20 articles.
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2. Characterization of the supernumerary chromosome in cat eye syndrome;McDermid;Science,1986
3. Genomic disorders on 22q11;McDermid;Am. J. Hum. Genet.,2002
4. Clinical characteristics of a sample of patients with cat eye syndrome;Rosa;Rev. Assoc. Med. Bras.,2010
5. Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease;Prieto;J. Pediatr. Surg.,2007
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2. Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases;American Journal of Medical Genetics Part A;2023-11-16
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4. Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study;Taiwanese Journal of Obstetrics and Gynecology;2023-01
5. Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome;Italian Journal of Pediatrics;2022-09-08
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