AUTHOR INDEX

A B C Ç D E F G H I İ J K L M N O Ö P R S Ş T U Ü V Y Z
Hazan

Filiz Hazan

Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3

(J Clin Res Pediatr Endocrinol 2012; 4: -)

A Case of Turner Syndrome with Concomitant 
Transient Hypogammaglobulinaemia of 
Infancy and Central Diabetes Insipidus

(J Clin Res Pediatr Endocrinol 2013; 5: -)

46,XY Complete Gonadal Dysgenesis: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

Screening of PROP-1, LHX2, and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

A Case with Acrodysostosis and Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)

Phenotype-Genotype Correlations in Bardet-Biedl Syndrome Patients with Molecular Analysis

(J Clin Res Pediatr Endocrinol 2015; 7: 82-82)

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 89-89)

PTPN11, SOS1, and BRAF Gene Mutation Spectrum in RASopathies in Molecular Diagnosis

(J Clin Res Pediatr Endocrinol 2017; 9: 25-25)

Investigation of Androgen Receptor Gen Mutation Spectrum in the Turkish Patients with Disorder of Sex Development

(J Clin Res Pediatr Endocrinol 2017; 9: 23-23)

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

(J Clin Res Pediatr Endocrinol 2017; 9: 21-21)

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 216-221)
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