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Huynh, Minh Tuan
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1

Antenatal ultrasound features of isolated recurrent copy nu..:

Courdier, Cécile ; Boudjarane, John ; Malan, Valérie...
Prenatal Diagnosis.  43 (2023)  6 - p. 734-745 , 2023
Link: https://doi.org/10.1002/..
 
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2

WAGR syndrome and congenital hypothyroidism in a child with..:

Huynh, Minh Tuan ; Boudry‐Labis, Elise ; Duban, Bénédicte...
American Journal of Medical Genetics Part A.  173 (2017)  6 - p. 1690-1693 , 2017
Link: https://doi.org/10.1002/..
 
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3

RUNX1T1, a chromatin repression protein, is a candidate gen..:

Huynh, Minh Tuan ; Béri‐Dexheimer, Mylène ; Bonnet, Céline...
American Journal of Medical Genetics Part A.  158A (2012)  7 - p. 1782-1784 , 2012
Link: https://doi.org/10.1002/..
 
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4

P199: Novel homozygous GLDC variants causing late-onset gly..:

Huynh, Minh-Tuan ; Landais, Emilie ; De Sainte Agathe, Jean-Madeleine..
Genetics in Medicine Open.  1 (2023)  1 - p. 100228 , 2023
Link: https://doi.org/10.1016/..
 
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5

P612: Application of prenatal exome sequencing in fetuses w..:

Huynh, Minh-Tuan ; Potel, Stéphanie ; Degre, Sophie...
Genetics in Medicine Open.  1 (2023)  1 - p. 100668 , 2023
Link: https://doi.org/10.1016/..
 
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6

Novel homozygous GLDC variant causing late-onset glycine en..:

Huynh, Minh-Tuan ; Landais, Emilie ; Agathe, Jean-Madeleine De Sainte...
Molecular Genetics and Metabolism Reports.  34 (2023)  - p. 100959 , 2023
Link: https://doi.org/10.1016/..
 
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7

AKAP9-Related Channelopathy: Novel Pathogenic Variant and R..:

Huynh, Minh-Tuan ; Proust, Alexis ; Bouligand, Jérôme.
Genes.  13 (2022)  11 - p. 2167 , 2022
Link: https://doi.org/10.3390/..
 
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8

eP456: Heterozygous deletion of the VEGFC gene in 4q34.3 is..:

Huynh, Minh-Tuan ; Degre, Sophie ; Breon, Cathy..
Genetics in Medicine.  24 (2022)  3 - p. S285-S287 , 2022
Link: https://doi.org/10.1016/..
 
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9

Novel interstitial 2q12.3q13 microdeletion predisposes to d..:

Huynh, Minh-Tuan ; Beneteau, Claire ; Marion, Gerard...
Molecular Genetics and Metabolism.  132 (2021)  - p. S222-S224 , 2021
Link: https://doi.org/10.1016/..
 
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10

Novel interstitial 2q12.3q13 microdeletion predisposes to d..:

Huynh, Minh-Tuan ; Gérard, Marion ; Ranguin, Kara...
neurogenetics.  22 (2021)  3 - p. 195-206 , 2021
Link: https://doi.org/10.1007/..
 
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11

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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12

Novel compound heterozygous TMEM67 variants in a Vietnamese..:

Bui, Thi Phuong Hoa ; Nguyen, Ngoc Tu ; Ngo, Van Doan...
BMC Medical Genetics.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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13

15q24.1 BP4-BP1 microdeletion unmasking paternally inherite..:

Huynh, Minh-Tuan ; Lambert, Anne-Sophie ; Tosca, Lucie...
European Journal of Medical Genetics.  61 (2018)  8 - p. 459-464 , 2018
Link: https://doi.org/10.1016/..
 
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14

First prenatal case of proximal 19p13.12 microdeletion synd..:

Huynh, Minh-Tuan ; Tosca, Lucie ; Petit, François...
European Journal of Medical Genetics.  61 (2018)  6 - p. 322-328 , 2018
Link: https://doi.org/10.1016/..
 
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15

A heterozygous microdeletion of 20q13.13 encompassing ADNP ..:

Huynh, Minh-Tuan ; Boudry-Labis, Elise ; Massard, Alfred...
European Journal of Human Genetics.  26 (2018)  10 - p. 1497-1501 , 2018
Link: https://doi.org/10.1038/..
 
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