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/vufind/Search/Results?lookfor=%22Mishra%2C+Puneeta%22&type=Person&sort=year
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PubPharm (6)
1
Faces of Fibrodysplasia Ossificans Progressiva : Lessons from a Clinical Masquerader
enthalten in:
Indian journal of pediatrics
| 2023
von
Gupta, A.
|
Mishra, P.
|
Chowdhury, M.
| +4
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2
The spectrum of neurological manifestations and genotype-phenotype correlation in Indian children with Gaucher disease
enthalten in:
American journal of medical genetics. Part A
| 2023
von
Venkatachari, M.
|
Chakraborty, S.
|
Correa, A.
| +9
ErratumIn: Am J Med Genet A. 2023 Jun 1;:. - PMID 37260296
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3
The spectrum of neurological manifestations and genotype–phenotype correlation in Indian children with Gaucher disease
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2023
von
Venkatachari, M.
|
Chakraborty, S.
|
Correa, A.
| +9
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4
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases
enthalten in:
Indian journal of pediatrics
| 2020
von
Correa, A.
|
Mishra, P.
|
Kabra, M.
| +1
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5
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases
enthalten in:
Indian journal of pediatrics
| 2020
von
Correa, A.
|
Mishra, P.
|
Kabra, M.
| +1
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6
Apert syndrome with congenital diaphragmatic hernia : another case report and review of the literature
enthalten in:
Clinical dysmorphology
| 2019
von
Kaur, R.
|
Mishra, P.
|
Kumar, S.
| +3
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1
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Indian journal of pediatrics
1
American Journal of Medical Genetics Part C: Se...
1
American journal of medical genetics. Part A
1
Clinical dysmorphology
Thema
4
Journal Article
2
Beckwith-Wiedemann syndrome
2
Case Reports
2
Epigenetics
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MS-MLPA
2
Overgrowth
1
ACVR1
1
EC 2.7.10.1
1
EC 3.2.1.45
1
FGFR2 protein, human
1
Fibrodysplasia ossificans progressiva
1
GBA 1
1
Glucosylceramidase
1
Heterotopic ossification
1
Misdiagnosis
1
Myositis ossificans
1
Receptor, Fibroblast Growth Factor, Type 2
1
Review
1
c.1448T>C
1
neurological Gaucher disease
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