Karimi-Nejad R - Search Results

1

Neu-Laxova syndrome: report of a case and comments.

Karimi-Nejad MH, Khajavi H, Gharavi MJ, Karimi-Nejad R. Karimi-Nejad MH, et al. Among authors: karimi nejad r. Am J Med Genet. 1987 Sep;28(1):17-23. doi: 10.1002/ajmg.1320280104. Am J Med Genet. 1987. PMID: 3314507 Review.

2

Blepharophimosis syndrome (BPES) and additional abnormalities in a female with a balanced X:3 translocation.

Karimi-Nejad A, Karimi-Nejad R, Najafi H, Karimi-Nejad MH. Karimi-Nejad A, et al. Among authors: karimi nejad r. Clin Dysmorphol. 1996 Jul;5(3):259-61. Clin Dysmorphol. 1996. PMID: 8818456 Review. No abstract available.

3

New findings in a patient with distal 13q-.

Karimi-Nejad A, Shafeghati Y, Karimi-Nejad R, Nabavi-Nia N, Kodoma K, Karimi-Nejad MH. Karimi-Nejad A, et al. Among authors: karimi nejad r. Clin Dysmorphol. 1998 Apr;7(2):153-4. doi: 10.1097/00019605-199804000-00015. Clin Dysmorphol. 1998. PMID: 9571290 No abstract available.

4

The beta-thalassemia mutation spectrum in the Iranian population.

Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. Najmabadi H, et al. Among authors: karimi nejad r. Hemoglobin. 2001 Aug;25(3):285-96. doi: 10.1081/hem-100105221. Hemoglobin. 2001. PMID: 11570721

5

Fourteen-year experience of prenatal diagnosis of thalassemia in Iran.

Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, Samavat A, Mehdipour E, Modell B, Kariminejad MH. Najmabadi H, et al. Community Genet. 2006;9(2):93-7. doi: 10.1159/000091486. Community Genet. 2006. PMID: 16612059

6

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. Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658. Haematologica. 2007. PMID: 17606454 Free article.

7

Genetic screening of leber congenital amaurosis in a large consanguineous Iranian family.

Rezaie T, Karimi-Nejad MH, Meshkat MR, Sohbati S, Karimi-Nejad R, Najmabadi H, Sarfarazi M. Rezaie T, et al. Among authors: karimi nejad r. Ophthalmic Genet. 2007 Dec;28(4):224-8. doi: 10.1080/13816810701663550. Ophthalmic Genet. 2007. PMID: 18161624

8

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. 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

9

11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features.

Kariminejad A, Kariminejad R, Tzschach A, Najafi H, Ahmed A, Ullmann R, Ropers HH, Kariminejad MH. Kariminejad A, et al. Am J Med Genet A. 2010 Oct;152A(10):2651-5. doi: 10.1002/ajmg.a.33623. Am J Med Genet A. 2010. PMID: 20799331 No abstract available.

10

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Kariminejad A, Kariminejad R, Moshtagh A, Zanganeh M, Kariminejad MH, Neuenschwander S, Okoniewski M, Wey E, Schinzel A, Baumer A. Kariminejad A, et al. Eur J Hum Genet. 2011 May;19(5):555-60. doi: 10.1038/ejhg.2010.252. Epub 2011 Feb 16. Eur J Hum Genet. 2011. PMID: 21326286 Free PMC article.

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