A clinical and molecular genetic study of 112 Iranian families with primary microcephaly
Darvish, H, Esmaeeli-Nieh, S, Monajemi, G B, Mohseni, M, Ghasemi-Firouzabadi, S, Abedini, S S, Bahman, I, Jamali, P, Azimi, S, Mojahedi, F, Dehghan, A, Shafeghati, Y, Jankhah, A, Falah, M, Soltani Banavandi, M J, Ghani-Kakhi, M, Garshasbi, M, Rakhshani, F, Naghavi, A, Tzschach, A, Neitzel, H, Ropers, H H, Kuss, A W, Behjati, F, Kahrizi, K, Najmabadi, H
Published in Journal of medical genetics (01.12.2010)
Published in Journal of medical genetics (01.12.2010)
Get full text
Journal Article
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB
Bicknell, Louise S, Farrington-Rock, Claire, Shafeghati, Yousef, Rump, Patrick, Alanay, Yasemin, Alembik, Yves, Al-Madani, Navid, Firth, Helen, Karimi-Nejad, Mohammad Hassan, Kim, Chong Ae, Leask, Kathryn, Maisenbacher, Melissa, Moran, Ellen, Pappas, John G, Prontera, Paolo, de Ravel, Thomy, Fryns, Jean-Pierre, Sweeney, Elizabeth, Fryer, Alan, Unger, Sheila, Wilson, L C, Lachman, Ralph S, Rimoin, David L, Cohn, Daniel H, Krakow, Deborah, Robertson, Stephen P
Published in Journal of medical genetics (01.02.2007)
Published in Journal of medical genetics (01.02.2007)
Get full text
Journal Article
LMNA mutations in atypical Werner's syndrome
Chen, Lishan, Lee, Lin, Kudlow, Brian A, Dos Santos, Heloisa G, Sletvold, Olav, Shafeghati, Yousef, Botha, Eleanor G, Garg, Abhimanyu, Hanson, Nancy B, Martin, George M, Mian, I Saira, Kennedy, Brian K, Oshima, Junko
Published in The Lancet (British edition) (09.08.2003)
Published in The Lancet (British edition) (09.08.2003)
Get full text
Journal Article
Tay-Sachs Disease; Report of 6 Iranian Patients and Review of Literature
Hadipour, Z., Shafeghati, Y., Tonekaboni, H., Verheijen, F.W., Rolfs, A., Hadipour, F.
Published in Dānishnāmah-i Ṣārim (Online) (01.01.2017)
Published in Dānishnāmah-i Ṣārim (Online) (01.01.2017)
Get full text
Journal Article
Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy
Hasanzad, Mandana, Golkar, Zahra, Kariminejad, Roxana, Hadavi, Valeh, Almadani, Navid, Afroozan, Fariba, Salahshurifar, Iman, Shafeghati, Yousef, Kahrizi, Kimia, Najmabadi, Hossein
Published in Annals of the Academy of Medicine, Singapore (01.02.2009)
Published in Annals of the Academy of Medicine, Singapore (01.02.2009)
Get full text
Journal Article
Evaluation of Methylation Status in the 5'UTR Promoter Region of the DBC2 Gene as a Biomarker in Sporadic Breast Cancer
Hajikhan Mirzaei, Mehri, Noruzinia, Mehrdad, Karbassian, Hamid, Shafeghati, Yousef, Keyhanee, Mousa, Bidmeshki-Pour, Ali
Published in Cell journal (Yakhteh) (01.01.2012)
Get full text
Published in Cell journal (Yakhteh) (01.01.2012)
Journal Article
Hereditary bilateral conductive hearing loss caused by total loss of ossicles: a report of familial expansile osteolysis
Daneshi, Ahmad, Shafeghati, Yousef, Karimi-Nejad, Mohammad Hassan, Khosravi, Amir, Farhang, Fariba
Published in Otology & neurotology (01.03.2005)
Published in Otology & neurotology (01.03.2005)
Get more information
Journal Article
Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia
Ghasemi Firoozabadi S, Shafeghati Y, Keyhani E, Kariminejad R, Oloomi Z, Moosavi F, Amini F, Najmabadi H, Behiati F
Published in Majallah-i Danishkadah-'i Pizishki (01.10.2007)
Get full text
Published in Majallah-i Danishkadah-'i Pizishki (01.10.2007)
Journal Article
Progeroid Syndrome and Mutation in LMNA Gene: Report of Two Cases from Iran
Y Shafeghati, N Levy, G.M Martin
Published in Journal of Kerman University of Medical Sciences (01.12.2005)
Get full text
Published in Journal of Kerman University of Medical Sciences (01.12.2005)
Journal Article
New findings in a patient with distal 13q
Karimi-Nejad, A, Shafeghati, Y, Karimi-Nejad, R, Nabavi-Nia, N, Kodoma, K, Karimi-Nejad, M H
Published in Clinical dysmorphology (01.04.1998)
Published in Clinical dysmorphology (01.04.1998)
Get more information
Journal Article
Cytogenetic analysis of 1284 cases of Down syndrome
M.H Kariminejhad, R Kariminejhad, F Azimi, N Nabavi nia, K Alavi, M.T Takyar, Y Shafeghati
Published in Journal of Kerman University of Medical Sciences (01.12.1997)
Get full text
Published in Journal of Kerman University of Medical Sciences (01.12.1997)
Journal Article