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Moradkhani, Kamran
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1

LHX2 haploinsufficiency causes a variable neurodevelopmenta..:

Schmid, Cosima M. ; Gregor, Anne ; Costain, Gregory...
Genetics in Medicine.  25 (2023)  7 - p. 100839 , 2023
Link: https://doi.org/10.1016/..
 
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2

Rare and de novo duplications containing TCF20 are associat..:

Lévy, Jonathan ; Cogan, Guillaume ; Maruani, Anna...
Clinical Genetics.  101 (2021)  3 - p. 364-370 , 2021
Link: https://doi.org/10.1111/..
 
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3

Structural abnormalities of chromosome 8 and fetoplacental ..:

Huynh, Minh-Tuan ; Riteau, Anne-Sophie ; Moradkhani, Kamran...
European Journal of Medical Genetics.  64 (2021)  1 - p. 104118 , 2021
Link: https://doi.org/10.1016/..
 
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4

11q24.2q24.3 microdeletion in two families presenting featu..:

Conrad, Solène ; Demurger, Florence ; Moradkhani, Kamran...
American Journal of Medical Genetics Part A.  179 (2019)  6 - p. 993-1000 , 2019
Link: https://doi.org/10.1002/..
 
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5

Morphokinetic parameters in chromosomal translocation carri..:

Lammers, Jenna ; Reignier, Arnaud ; Splingart, Carole...
Reproductive BioMedicine Online.  38 (2019)  2 - p. 177-183 , 2019
Link: https://doi.org/10.1016/..
 
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6

Risk estimation of uniparental disomy of chromosome 14 or 1..:

Moradkhani, Kamran ; Cuisset, Laurence ; Boisseau, Pierre...
Prenatal Diagnosis.  39 (2019)  11 - p. 986-992 , 2019
Link: https://doi.org/10.1002/..
 
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7

Variable neurodevelopmental and morphological phenotypes of..:

Myers, Lynnea ; Blyth, Moira ; Moradkhani, Kamran...
Molecular Genetics & Genomic Medicine.  8 (2019)  1 - p. , 2019
Link: https://doi.org/10.1002/..
 
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8

Prenatal findings in 1p36 deletion syndrome: New cases and ..:

Guterman, Sarah ; Beneteau, Claire ; Redon, Sylvia...
Prenatal Diagnosis.  39 (2019)  10 - p. 871-882 , 2019
Link: https://doi.org/10.1002/..
 
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9

Pitfalls in the genetic diagnosis of Hb S:

Moradkhani, Kamran ; Riou, Jean ; Wajcman, Henri
Clinical Biochemistry.  46 (2013)  4-5 - p. 291-299 , 2013
Link: https://doi.org/10.1016/..
 
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10

Updates of the HbVar database of human hemoglobin variants ..:

Giardine, Belinda ; Borg, Joseph ; Viennas, Emmanouil...
Nucleic Acids Research.  42 (2013)  D1 - p. D1063-D1069 , 2013
Link: https://doi.org/10.1093/..
 
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11

Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.30..:

Benmansour, Ikbel ; Moradkhani, Kamran ; Moumni, Imen...
Blood Cells, Molecules, and Diseases.  50 (2013)  2 - p. 110-114 , 2013
Link: https://doi.org/10.1016/..
 
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12

Glucose-6-phosphate dehydrogenase (G6PD) mutations database..:

Minucci, Angelo ; Moradkhani, Kamran ; Hwang, Ming Jing...
Blood Cells, Molecules, and Diseases.  48 (2012)  3 - p. 154-165 , 2012
Link: https://doi.org/10.1016/..
 
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13

Practical approach for characterization of glucose 6‐phosph..:

Moradkhani, Kamran ; Mekki, Chadia ; Bahuau, Michel...
American Journal of Hematology.  87 (2011)  2 - p. 208-210 , 2011
Link: https://doi.org/10.1002/..
 
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14

Molecular characterization of glucose-6-phosphate dehydroge..:

Al-Jaouni, Soad K ; Jarullah, Jummanah ; Azhar, Essam.
BMC Research Notes.  4 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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15

Systematic documentation and analysis of human genetic vari..:

Giardine, Belinda ; Borg, Joseph ; Higgs, Douglas R...
Nature Genetics.  43 (2011)  4 - p. 295-301 , 2011
Link: https://doi.org/10.1038/..
 
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