Karimi-Nejad A - Search Results

1

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. Clin Dysmorphol. 1998 Apr;7(2):153-4. doi: 10.1097/00019605-199804000-00015. Clin Dysmorphol. 1998. PMID: 9571290 No abstract available.

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. Clin Dysmorphol. 1996 Jul;5(3):259-61. Clin Dysmorphol. 1996. PMID: 8818456 Review. No abstract available.

3

Supernumerary nipples in a Bartsocas-Papas patient in a consanguineous Iranian family.

Shafeghati Y, Karimi-Nejad A, Karimi-Nejad R. Shafeghati Y, et al. Among authors: karimi nejad a. Clin Dysmorphol. 1999 Apr;8(2):155-6. doi: 10.1097/00019605-199904000-00014. Clin Dysmorphol. 1999. PMID: 10319208

4

Skull defects, alopecia and distinctive facies: a new syndrome?

Kariminejad A, Bozorgmehr B, Ashrafi MR, Kariminejad MH. Kariminejad A, et al. Clin Dysmorphol. 2008 Jul;17(3):203-205. doi: 10.1097/MCD.0b013e3282fba59d. Clin Dysmorphol. 2008. PMID: 18541970 No abstract available.

5

Clinical variability in acro-cardio-facial-syndrome.

Kariminejad A, Bozorgmehr B, Sedighi Gilani MA, Almadani N, Kariminejad MH. Kariminejad A, et al. Am J Med Genet A. 2008 Aug 1;146A(15):1977-9. doi: 10.1002/ajmg.a.32052. Am J Med Genet A. 2008. PMID: 18627040

6

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

7

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.

8

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.

9

An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndrome.

Kariminejad A, Ghaderi-Sohi S, Kariminejad MH, Lachman R. Kariminejad A, et al. Fetal Pediatr Pathol. 2012 Oct;31(5):295-9. doi: 10.3109/15513815.2012.659386. Epub 2012 Mar 20. Fetal Pediatr Pathol. 2012. PMID: 22432872

10

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders.

Abdelfattah F, Kariminejad A, Kahlert AK, Morrison PJ, Gumus E, Mathews KD, Darbro BW, Amor DJ, Walsh M, Sznajer Y, Weiß L, Weidensee S, Chitayat D, Shannon P, Bermejo-Sánchez E, Riaño-Galán I, Hayes I, Poke G, Rooryck C, Pennamen P, Khung-Savatovsky S, Toutain A, Vuillaume ML, Ghaderi-Sohi S, Kariminejad MH, Weinert S, Sticht H, Zenker M, Schanze D. Abdelfattah F, et al. Hum Mutat. 2020 Sep;41(9):1615-1628. doi: 10.1002/humu.24067. Epub 2020 Jul 15. Hum Mutat. 2020. PMID: 32579715

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