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Mahdieh, Nejat
42
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1
Neurofibromatosis-Noonan syndrome and growth deficiency in ..:
Dalili, Setila
;
Hoseini Nouri, Seyyedeh Azade
;
Bayat, Reza
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940353/. , 2023
Link:
http://www.ncbi.nlm.nih...
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2
Expanding the genetic spectrum of giant axonal neuropathy: ..:
Ashrafi, Mahmoud Reza
;
Dehnavi, Ali Zare
;
Tavasoli, Ali Reza
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265088/. , 2023
Link:
http://www.ncbi.nlm.nih...
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3
TCAP gene is not a common cause of cardiomyopathy in Irania..:
Alaei, Zahra
;
Zamani, Nasrin
;
Rabbani, Bahareh
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523715/. , 2023
Link:
http://www.ncbi.nlm.nih...
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4
Determinants of perivascular adipose tissue stranding as a ..:
Pouraliakbar, Hamidreza
;
Abouie, Abolfazl
;
Ziaeifar, Elham
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086606/. , 2023
Link:
http://www.ncbi.nlm.nih...
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5
A novel stop-gain pathogenic variant in the KCNQ1 gene caus..:
Kalayinia, Samira
;
Dalili, Mohammad
;
Pourirahim, Maryam
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835262/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
6
Determinants of perivascular adipose tissue stranding as a ..:
Pouraliakbar, Hamidreza
;
Abouie, Abolfazl
;
Ziaeifar, Elham
...
Polish Journal of Radiology, T. 88, s. e141-e148. , 2023
Link:
https://ruj.uj.edu.pl/xm..
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7
Genetic testing of leukodystrophies unraveling extensive he..:
Mahdieh, Nejat
;
Soveizi, Mahdieh
;
Tavasoli, Ali Reza
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864965/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
8
A novel pathogenic variant of SRD5A2 in an Iranian psuedohe..:
Dalili, Setilla
;
Rabbani, Bahareh
;
Hassanzadeh Rad, Afagh
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562857/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
9
HBB mutations and HbA2 level: Escaping the carrier screenin..:
Sharifi, Ameneh
;
Mahdieh, Nejat
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869310/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
10
GATA4 screening in Iranian patients of various ethnicities ..:
Kalayinia, Samira
;
Maleki, Majid
;
Rokni‐Zadeh, Hassan
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757118/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
11
A novel de novo dominant mutation of NOTCH1 gene in an Iran..:
Kalayinia, Samira
;
Maleki, Majid
;
Mahdavi, Mohammad
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171333/. , 2019
Link:
http://www.ncbi.nlm.nih...
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12
Genotypic effect of a mutation of the MYBPC3 gene and two p..:
Mahdieh, Nejat
;
Hosseini Moghaddam, Maryam
;
Motavaf, Mahsa
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817065/. , 2018
Link:
http://www.ncbi.nlm.nih...
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13
A novel PKP2 mutation and intrafamilial phenotypic variabil..:
Mahdieh, Nejat
;
Saedi, Sedigheh
;
Soveizi, Mahdieh
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025913/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
14
Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart..:
Kalayinia, Samira
;
Shahani, Tina
;
Biglari, Alireza
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938395/. , 2018
Link:
http://www.ncbi.nlm.nih...
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15
Novel Pathogenic Variants Underlie SLC26A4-related Hearing ..:
Cengiz, Filiz Basak
;
Yilmazer, Rasim
;
Olgun, Levent
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679420/. , 2017
Link:
http://www.ncbi.nlm.nih...
1-15