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Page 1
Lost in translation: limitations of a universal approach in genetic counseling.
J Genet Couns. 2010 Feb;19(1):5-6. doi: 10.1007/s10897-009-9255-7. Epub 2009 Oct 3.
J Genet Couns. 2010.
PMID: 19802691
No abstract available.
Genetic counseling in carriers of reciprocal translocations involving two autosomes.
Pourjafari B, Pour-Jafari H, Farimani M, Ghahramani S, Saleh EK.
Pourjafari B, et al. Among authors: pour jafari h.
Indian J Hum Genet. 2012 May;18(2):250-3. doi: 10.4103/0971-6866.100802.
Indian J Hum Genet. 2012.
PMID: 23162307
Free PMC article.
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High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.
Chaleshtori MH, Farrokhi E, Shahrani M, Kheiri S, Dolati M, Rad LH, Pour-Jafari H, Samani KG, Chaleshtori KS, Crosby AH.
Chaleshtori MH, et al. Among authors: pour jafari h.
Int J Pediatr Otorhinolaryngol. 2007 Jun;71(6):863-7. doi: 10.1016/j.ijporl.2007.02.005. Epub 2007 Apr 10.
Int J Pediatr Otorhinolaryngol. 2007.
PMID: 17428550
Free article.
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Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.
Elahi E, Kalhor R, Banihosseini SS, Torabi N, Pour-Jafari H, Houshmand M, Amini SS, Ramezani A, Loeys B.
Elahi E, et al. Among authors: pour jafari h.
J Invest Dermatol. 2006 Jul;126(7):1506-9. doi: 10.1038/sj.jid.5700247. Epub 2006 May 11.
J Invest Dermatol. 2006.
PMID: 16691202
Free article.
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A survey of (CAG)n repeats causing juvenile Huntington disease in an Iranian family with 4 affected members.
Mazdeh M, Pour-Jafari H, Ghaleiha A, Pour-Jafari B.
Mazdeh M, et al. Among authors: pour jafari h.
Neurosciences (Riyadh). 2009 Jul;14(3):273-6.
Neurosciences (Riyadh). 2009.
PMID: 21048629
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