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PubPharm (31)
1
Congenital Dyserythropoietic Anemia Type II : High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population
enthalten in:
Indian journal of pediatrics
| 2023
von
Saptarshi, A.
|
More, T.
|
Dongerdiye, R.
| +1
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2
Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population
enthalten in:
Italian journal of pediatrics
| 2023
von
Saptarshi, A.
|
Dongerdiye, R.
|
More, T.
| +1
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3
Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population
enthalten in:
The Italian journal of pediatrics
| 2023
von
Saptarshi, A.
|
Dongerdiye, R.
|
More, T.
| +1
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4
Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population
enthalten in:
Indian journal of pediatrics
| 2023
von
Saptarshi, A.
|
More, T.
|
Dongerdiye, R.
| +1
Wird geladen...
5
Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population
enthalten in:
Indian journal of pediatrics
| 2023
von
Saptarshi, A.
|
More, T.
|
Dongerdiye, R.
| +1
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6
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
enthalten in:
Annals of hematology
| 2023
von
Dongerdiye, R.
|
Bokde, M.
|
More, T.
| +5
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7
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
enthalten in:
Annals of hematology
| 2023
von
Dongerdiye, R.
|
Bokde, M.
|
More, T.
| +5
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8
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
enthalten in:
Annals of hematology
| 2023
von
Dongerdiye, R.
|
Bokde, M.
|
More, T.
| +5
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9
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients : expanding the molecular and clinical spectrum
enthalten in:
Molecular genetics and genomics : MGG
| 2023
von
More, T.
|
Devendra, R.
|
Dongerdiye, R.
| +2
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10
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum
enthalten in:
Molecular genetics and genomics
| 2023
von
More, T.
|
Devendra, R.
|
Dongerdiye, R.
| +2
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Medienart
31
Aufsätze
25
E-Artikel
25
E-Ressourcen
6
Gedruckte Aufsätze
Zeitschriftentitel
7
Annals of hematology
7
International journal of hematology
5
Indian journal of pediatrics
3
Journal of clinical pathology
2
BMC medical genomics
2
Molecular genetics and genomics
1
Hematology (Amsterdam, Netherlands)
1
Italian journal of pediatrics
1
Molecular genetics and genomics : MGG
1
ResearchSquare.com
1
The Italian journal of pediatrics
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Thema
12
Journal Article
12
Next-generation sequencing
10
India
10
Molecular modeling
4
Congenital anemia
4
EC 5.3.1.9
4
Erythroenzymopathies
4
Glucose-6-Phosphate Isomerase
4
Hereditary xerocytosis
4
Mechanosensitive Piezo1 ionic channels protein
4
Membranopathies
4
Molecular genetics
3
Ankyrin
3
Case Reports
3
Chronic non-spherocytic hemolytic anemia
3
EC 2.7.1.40
3
Frameshift
3
Genetic analysis
3
Glucose phosphate isomerase deficiency
3
Hemolytic anemia
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Erscheinungszeitraum
23
2020-
8
2010-2019
Erscheinungsjahr(e)
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Sprache
31
Englisch
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