Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures

Q1

AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES (ISSN: 19447558) , vol. 115 , pp. 433-443

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa

Q1

MOLECULAR VISION , vol. 16 , pp. 2753-2759

Tumor risk in disorders of sex development

Q1

SEXUAL DEVELOPMENT (ISSN: 16615425) , vol. 4 , pp. 259-269

Lack of correlation between phenotype and genotype in untreated 21-hydroxylase-deficient Indonesian patients

Q1

CLINICAL ENDOCRINOLOGY (ISSN: 03000664) , vol. 71 , pp. 628-635

Functional analysis of novel androgen receptor mutations in a unique cohort of Indonesian patients with a disorder of sex development

Q1

SEXUAL DEVELOPMENT (ISSN: 16615425) , vol. 3 , pp. 237-244

Gonadoblastoma arising in undifferentiated gonadal tissue within dysgenetic gonads

Q1

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM (ISSN: 0021972X) , vol. 91 , pp. 2404-2413

Increased PAI-1 plasma levels and risk of death from dengue: No association with the 4G/5G promoter polymorphism

Q3

THROMBOSIS JOURNAL (ISSN: 14779560) , vol. 3

Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asia populations

Q1

ANNALS OF HUMAN GENETICS (ISSN: 00034800) , vol. 65 , pp. 127-135

Genetic diversity at the FMR1 locus in the Indonesian population

Q1

ANNALS OF HUMAN GENETICS (ISSN: 00034800) , vol. 64 , pp. 329-339

Molecular screening for fragile X syndrome among Indonesian children with developmental disability [7]

NQ

AMERICAN JOURNAL OF MEDICAL GENETICS (ISSN: 01487299) , vol. 83 , pp. 350-351