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Journal of Medical Case Reports|May 4, 2026
Prenatal diagnosis of congenital diaphragmatic hernia with mosaicism of chromosomes 17q and 18q in Iran: a case reportArezou Heydari, Zahra Rezvani, Mohamad Ali DowlatiWorld Journal of Plastic Surgery|July 17, 2019
Correction of Severe Deviated Nose by Intermediate Short OsteotomyRohollah Abbasi, Ali Dowlati, Mohamad Ali Seif Rabiei, et al.Mitochondrial DNA|September 18, 2012
Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case studyMohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.Molecular Biology Reports|December 18, 2012
Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing lossMohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.Gene|December 4, 2012
Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findingsAzadeh Shojaei, Farkhondeh Behjati, Pupak Derakhshandeh-Peykar, et al.Pageof 1