Publications by authors named "Valeh Hadavi"

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Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.
Parvin Rostami, Sahar Valizadegan, Maryam Ghalandary, Mana M Mehrjouy, Giti Esmail-Nia, Valeh Hadavi

Arch Iran Med· May 2015

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Characterizing a cohort of α-thalassemia couples collected during screening for hemoglobinopathies: 14 years of an Iranian experience.
Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi

Hemoglobin· February 2015

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Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran.
Mohammad Reza Mahdavi, Nooshin Bayat, Valeh Hadavi, Hosein Karami, Payam Roshan

J Pak Med Assoc· April 2012

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Hossein Najmabadi, Hao Hu, Masoud Garshasbi, Tomasz Zemojtel, Seyedeh Sedigheh Abedini, Valeh Hadavi

Nature· September 2011

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Genotype-phenotype correlation in Iranian patients with Hb H disease.
Saedieh Ebrahimkhani, Azita Azarkeivan, Nooshin Bayat, Mahdieh Houry-Parvin, Sayeh Jalil-Nejad, Valeh Hadavi

Hemoglobin· June 2011

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Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.
Andreas Walter Kuss, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Farkhondeh Behjati, Valeh Hadavi

Hum Genet· February 2011

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A report of 8 cases with hemoglobin H disease in an Iranian family.
Azita Azarkeivan, Maryam Neishabury, Valeh Hadavi, Fatemehsadat Esteghamat, Saideh Enrahimkhani

Pediatr Hematol Oncol· August 2010

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Alpha-thalassemia mutations in Gilan Province, North Iran.
Valeh Hadavi, Maryam Jafroodi, Nima Hafezi-Nejad, Sousan Dehnadi Moghadam, Fatemeh Eskandari

Hemoglobin· February 2010

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alpha-Thalassemia mutation analyses in Mazandaran province, North Iran.
Ahmad Tamaddoni, Valeh Hadavi, Nima Hafezi Nejad, Atefeh Khosh-Ain, Rita Siami

Hemoglobin· June 2009

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Prenatal diagnosis for beta-thalassemia major in the Iranian Province of Hormozgan.
Pooneh Nikuei, Valeh Hadavi, Minoo Rajaei, Mozhgan Saberi, Fozieh Hajizade

Hemoglobin· February 2009

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alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
Khodamorad Zandian, Jamal Nateghi, Bijan Keikhaie, Mohammad Pedram, Nima Hafezi-Nejad, Valeh Hadavi

Hemoglobin· February 2009

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Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy.
Mandana Hasanzad, Zahra Golkar, Roxana Kariminejad, Valeh Hadavi, Navid Almadani

Ann Acad Med Singap· February 2009

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A defect in the TUSC3 gene is associated with autosomal recessive mental retardation.
Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad

Am J Hum Genet· May 2008

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Double de novo mutations of ELA2 in cyclic and severe congenital neutropenia.
Stephen J Salipante, Kathleen F Benson, Joanna Luty, Valeh Hadavi, Roxana Kariminejad

Hum Mutat· September 2007

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Elucidating the spectrum of alpha-thalassemia mutations in Iran.
Valeh Hadavi, Amir Hossein Taromchi, Mahdi Malekpour, Behjat Gholami, Hai-Yang Law

Haematologica· July 2007

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Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
Hossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Valeh Hadavi

Hum Genet· March 2007

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Fourteen-year experience of prenatal diagnosis of thalassemia in Iran.
Hossein Najmabadi, Alireza Ghamari, Farhad Sahebjam, Roxana Kariminejad, Valeh Hadavi

Community Genet· September 2006

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