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/vufind/Search/Results?lookfor=%22Jamwal%2C+Manu%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Jamwal%2C+Manu%22&type=Person&sort=year
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PubPharm (74)
1
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II : a diagnostic pitfall
enthalten in:
Journal of clinical pathology
| 2024
von
Jamwal, M.
|
Sreedharanunni, S.
|
Taak, R.
| +7
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2
Unearthing the genotype-inhibitor phenotype association in severe haemophilia A : A north Indian cohort study
enthalten in:
Haemophilia : the official journal of the World Federation of Hemophilia
| 2024
von
Ray, D.
|
Sharma, R.
|
Kumar, N.
| +7
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3
The frequency and clinical outcome of mono-hit and multi-hit TP53 aberrations in newly diagnosed multiple myeloma
enthalten in:
Pathology
| 2024
von
Sreedharanunni, S.
|
Singla, S.
|
Balakrishnan, A.
| +10
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4
Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic Setting
enthalten in:
The Journal of molecular diagnostics : JMD
| 2024
von
Sharma, P.
|
Bhatia, P.
|
Singh, M.
| +8
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5
First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia
enthalten in:
International journal of laboratory hematology
| 2023
von
Singh, N.
|
Bhatia, P.
|
Jamwal, M.
| +5
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6
Dehydrated hereditary stomatocytosis masquerading as primary haemochromatosis : a diagnostic challenge
enthalten in:
Pathology
| 2023
von
Jamwal, M.
|
Singh, N.
|
Sharma, P.
| +4
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7
Correction to : Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency
enthalten in:
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
| 2023
von
Sharma, R.
|
Jamwal, M.
|
Singh, N.
| +8
ErratumFor: Indian J Hematol Blood Transfus. 2023 Apr;39(2):276-283. - PMID 37006978
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8
Women in Selected Communities of Punjab, India Have a High Prevalence of Iron, Zinc, Vitamin B12, and Folate Deficiencies : Implications for a Multiply-Fortified Salt Intervention
enthalten in:
Nutrients
| 2023
von
Goh, Y.
|
Manger, M.
|
Duggal, M.
| +14
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9
Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency
enthalten in:
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
| 2023
von
Sharma, R.
|
Jamwal, M.
|
Singh, N.
| +8
ErratumIn: Indian J Hematol Blood Transfus. 2023 Jul;39(3):519-521. - PMID 37304469
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10
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect
enthalten in:
Haemophilia : the official journal of the World Federation of Hemophilia
| 2023
von
Sharma, R.
|
Jamwal, M.
|
Senee, H.
| +9
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Annals of hematology
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Indian journal of hematology & blood transfusio...
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Acta cardiologica
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26
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17
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6
Next-generation sequencing
5
Hemoglobins, Abnormal
4
Glanzmann thrombasthenia
4
Molecular diagnosis
4
Platelet function disorders
3
9001-27-8
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Blood Proteins
3
Factor VIII
3
Hemoglobinopathy
3
Hemolytic anemia
3
Micronutrients
3
haemolytic anaemia
2
12634-43-4
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9034-79-1
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Fortification
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GATA1 Transcription Factor
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Erscheinungszeitraum
54
2020-
20
2010-2019
Erscheinungsjahr(e)
Von:
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Sprache
66
Englisch
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