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Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
Int J Mol Sci. 2017 Mar 15;18(3):635. doi: 10.3390/ijms18030635.
Int J Mol Sci. 2017.
PMID: 28294978
Free PMC article.
Review.
Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: association of extra copy of MSX2 with craniosynostosis.
Kariminejad A, Kariminejad R, Tzschach A, Ullmann R, Ahmed A, Asghari-Roodsari A, Salehpour S, Afroozan F, Ropers HH, Kariminejad MH.
Kariminejad A, et al. Among authors: afroozan f.
Am J Med Genet A. 2009 Jul;149A(7):1544-9. doi: 10.1002/ajmg.a.32949.
Am J Med Genet A. 2009.
PMID: 19533795
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Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.
Rostami P, Valizadegan S, Ghalandary M, Mehrjouy MM, Esmail-Nia G, Khalili S, Shahmoradi SS, Imanian H, Hadavi V, Ghaderi-Sohi S, Almadani N, Afroozan F, Kariminejad A, Kariminejad R, Najmabadi H.
Rostami P, et al. Among authors: afroozan f.
Arch Iran Med. 2015 May;18(5):296-303.
Arch Iran Med. 2015.
PMID: 25959911
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TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor.
Kariminejad A, Dahl-Halvarsson M, Ravenscroft G, Afroozan F, Keshavarz E, Goullée H, Davis MR, Faraji Zonooz M, Najmabadi H, Laing NG, Tajsharghi H.
Kariminejad A, et al. Among authors: afroozan f.
Brain. 2017 Nov 1;140(11):2851-2859. doi: 10.1093/brain/awx230.
Brain. 2017.
PMID: 29053766
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Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H.
Abolhassani A, et al. Among authors: afroozan f.
NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0.
NPJ Genom Med. 2024.
PMID: 38374194
Free PMC article.
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Elucidating the spectrum of alpha-thalassemia mutations in Iran.
Hadavi V, Taromchi AH, Malekpour M, Gholami B, Law HY, Almadani N, Afroozan F, Sahebjam F, Pajouh P, Kariminejad R, Kariminejad MH, Azarkeivan A, Jafroodi M, Tamaddoni A, Puehringer H, Oberkanins C, Najmabadi H.
Hadavi V, et al. Among authors: afroozan f.
Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658.
Haematologica. 2007.
PMID: 17606454
Free article.
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Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy.
Hasanzad M, Golkar Z, Kariminejad R, Hadavi V, Almadani N, Afroozan F, Salahshurifar I, Shafeghati Y, Kahrizi K, Najmabadi H.
Hasanzad M, et al. Among authors: afroozan f.
Ann Acad Med Singap. 2009 Feb;38(2):139-41.
Ann Acad Med Singap. 2009.
PMID: 19271042
Free article.
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