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Search Results - Akhtar, Ambrin
Search Results - Akhtar, Ambrin
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Scrub Typhus Presenting as Acute Flaccid Paralysis in a Child: A Differential to Be Included in a Common Presentation
by
Kumar, Pradeep
,
Prasad, Arun
,
Kumar, Subhash
,
Akhtar, Ambrin
Published in
Curēus (Palo Alto, CA)
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Vertical transmission and clinical outcome of the neonates born to SARS-CoV-2-positive mothers: a tertiary care hospital-based observational study
by
Kumar, Pradeep
,
Fadila
,
Prasad, Arun
,
Akhtar, Ambrin
,
Chaudhary, Bhabesh Kant
,
Tiwari, Lokesh Kumar
,
Chaudhry, Neha
Published in
BMJ paediatrics open
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Nanoengineering of mono (Au, Ag) and bimetallic (Ag-Au) alloy nanoparticles for dye degradation and toxicity assessment
by
Sabahat, Sana
,
Nazish, Yumna
,
Akhtar, Ambrin
,
Shahid, Ammara
Published in
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Scrub Typhus Presenting as Acute Flaccid Paralysis in a Child: A Differential to Be Included in a Common Presentation
by
Kumar, Pradeep
,
Prasad, Arun
,
Kumar, Subhash
,
Akhtar, Ambrin
Published in
Cureus
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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
by
Fatima, Ambrin
,
Hoeber, Jan
,
Schuster, Jens
,
Koshimizu, Eriko
,
Maya-Gonzalez, Carolina
,
Keren, Boris
,
Mignot, Cyril
,
Akram, Talia
,
Ali, Zafar
,
Miyatake, Satoko
,
Tanigawa, Junpei
,
Koike, Takayoshi
,
Kato, Mitsuhiro
,
Murakami, Yoshiko
,
Abdullah, Uzma
,
Ali, Muhammad Akhtar
,
Fadoul, Rein
,
Laan, Loora
,
Castillejo-López, Casimiro
,
Liik, Maarika
,
Jin, Zhe
,
Birnir, Bryndis
,
Matsumoto, Naomichi
,
Baig, Shahid M.
,
Klar, Joakim
,
Dahl, Niklas
Published in
American journal of human genetics
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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
by
Fatima, Ambrin
,
Hoeber, Jan
,
Schuster, Jens
,
Koshimizu, Eriko
,
Maya-Gonzalez, Carolina
,
Keren, Boris
,
Mignot, Cyril
,
Akram, Talia
,
Ali, Zafar
,
Miyatake, Satoko
,
Tanigawa, Junpei
,
Koike, Takayoshi
,
Kato, Mitsuhiro
,
Murakami, Yoshiko
,
Abdullah, Uzma
,
Ali, Muhammad Akhtar
,
Fadoul, Rein
,
Laan, Loora
,
Castillejo-López, Casimiro
,
Liik, Maarika
,
Jin, Zhe
,
Birnir, Bryndis
,
Matsumoto, Naomichi
,
Baig, Shahid M.
,
Klar, Joakim
,
Dahl, Niklas
Published in
American journal of human genetics
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Mono-allelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
by
Fatima, Ambrin
,
Hoeber, Jan
,
Schuster, Jens
,
Koshimizu, Eriko
,
Maya-Gonzalez, Carolina
,
Keren, Boris
,
Mignot, Cyril
,
Akram, Talia
,
Ali, Zafar
,
Miyatake, Satoko
,
Tanigawa, Junpei
,
Koike, Takayoshi
,
Kato, Mitsuhiro
,
Murakami, Yoshiko
,
Abdullah, Uzma
,
Ali, Muhammad Akhtar
,
Fadoul, Rein
,
Laan, Loora
,
Castillejo-López, Casimiro
,
Liik, Maarika
,
Jin, Zhe
,
Birnir, Bryndis
,
Matsumoto, Naomichi
,
Baig, Shahid M
,
Klar, Joakim
,
Dahl, Niklas
Published in
American journal of human genetics
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Article
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