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Mittal, Balraj
414  results:
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1

A Fatal Case of 3‐Hydroxyisobutyryl‐CoA Hydrolase Deficienc..:

Puvabanditsin, Surasak ; Lee, Ian ; Cordero, Natasha...
Case Reports in Genetics.  2024 (2024)  1 - p. , 2024
Link: https://doi.org/10.1155/..
 
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2

Quadruple Primary Malignancies over 2 Years with Germline M..:

Aminian, Solaleh ; Al-Alloosh, Fawaz ; Yadegari, Fatemeh...
Case Reports in Genetics.  2024 (2024)  1 - p. , 2024
Link: https://doi.org/10.1155/..
 
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3

Discovery of a Novel DYRK1A Mutation (c.524del) in Intellec..:

Whitaker, Fiona ; Serrano, Alvaro ; Mittal, Balraj
Case Reports in Genetics.  2024 (2024)  1 - p. , 2024
Link: https://doi.org/10.1155/..
 
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4

Molecular diagnosis, drivers, and treatment modalities for ..:

, In: Biomarkers in Cancer Detection and Monitoring of Therapeutics,
Yadav, Saurabh ; Mittal, Balraj - p. 235-248 , 2024
Link: https://doi.org/10.1016/..
 
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5

Contributors:

, In: Biomarkers in Cancer Detection and Monitoring of Therapeutics,
Acharya, Chandan Kumar ; Adhikari, Madhuchhanda ; Adhikari, Suman... - p. xiii-xix , 2024
Link: https://doi.org/10.1016/..
 
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6

A Novel Heterozygous De Novo MORC2 Missense Variant Causes ..:

Arbide, Daniel ; Elkhateeb, Nour ; Goljan, Ewa...
Case Reports in Genetics.  2024 (2024)  - p. 1-5 , 2024
Link: https://doi.org/10.1155/..
 
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7

Mosaicism in BRPF1-Related Neurodevelopmental Disorder: Rep..:

Bayanbold, Khaliunaa ; Younger, Georgianne ; Darbro, Benjamin..
Case Reports in Genetics.  2023 (2023)  - p. 1-6 , 2023
Link: https://doi.org/10.1155/..
 
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8

A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication ..:

Bajracharya, Luna ; Lall, Meena ; Bijarnia-Mahay, Sunita...
Case Reports in Genetics.  2023 (2023)  - p. 1-9 , 2023
Link: https://doi.org/10.1155/..
 
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9

Recurrent Ischemic Strokes due to Monogenic COL4A1 Mutation..:

Wong-Valenzuela, Emilio Israel ; San Juan, Daniel ; Santos Zambrano, José...
Case Reports in Genetics.  2023 (2023)  - p. 1-4 , 2023
Link: https://doi.org/10.1155/..
 
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10

Manifestations of Intellectual Disability, Dystonia, and Pa..:

Arvio, Maria ; Lähdetie, Jaana ; Koivu, Hannu...
Case Reports in Genetics.  2023 (2023)  - p. 1-5 , 2023
Link: https://doi.org/10.1155/..
 
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11

Novel TTN Mutation Causing Severe Congenital Myopathy and U..:

Balasundaram, Palanikumar ; Avulakunta, Indirapriya Darshini ; Delfiner, Leslie...
Case Reports in Genetics.  2023 (2023)  - p. 1-4 , 2023
Link: https://doi.org/10.1155/..
 
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12

A Case of Congenital Hypotonia and Developmental Delay in a..:

Makarova, Elizaveta ; Legro, Nicole R. ; Aliu, Ermal.
Case Reports in Genetics.  2023 (2023)  - p. 1-5 , 2023
Link: https://doi.org/10.1155/..
 
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13

45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary A..:

Han, Yu ; Wu, Jiebin ; Tan, Fangfang...
Case Reports in Genetics.  2023 (2023)  - p. 1-5 , 2023
Link: https://doi.org/10.1155/..
 
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14

Prenatal Lethal Diagnosis of 8p23.1 Duplication Syndrome As..:

Hicks, Melissa A. ; Ebrahim, Salah ; Gonik, Bernard.
Case Reports in Genetics.  2023 (2023)  - p. 1-4 , 2023
Link: https://doi.org/10.1155/..
 
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15

A Rare 46,X,t(Y;10)(q12;p14) Balanced Translocation in Non-..:

Jahan Syeeda Khursheed, Kousar ; Rahman Kaleemullah, Mohammed ; Joseph, Annu...
Case Reports in Genetics.  2023 (2023)  - p. 1-4 , 2023
Link: https://doi.org/10.1155/..
 
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