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/vufind/Search/Results?lookfor=%22Verma%2C+I+C%22&type=Person&sort=year
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PubPharm (395)
1
Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene
enthalten in:
Indian journal of pediatrics
| 2022
von
Takkar, A.
|
Arora, V.
|
Saxena, R.
| +2
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2
Computational biology insights into genotype-clinical phenotype-protein phenotype relationships between novel SLC26A2 variants identified in inherited skeletal dysplasias
enthalten in:
European journal of medical genetics
| 2022
von
Biji, I.
|
Yadav, S.
|
Kulshrestha, S.
| +5
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3
Erratum to: Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India
enthalten in:
Indian pediatrics
| 2022
von
Singh, K.
|
Puri, R.
|
Bijarnia-Mahay, S.
| +7
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4
Erratum to: Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India
enthalten in:
Indian pediatrics
| 2022
von
Singh, K.
|
Puri, R.
|
Bijarnia-Mahay, S.
| +7
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5
Molecular studies in familial dilated cardiomyopathy - A pilot study
enthalten in:
International journal of cardiology. Heart & vasculature
| 2022
von
Mori, V.
|
Sawhney, J.
|
Verma, I.
| +9
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6
Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India
enthalten in:
Indian pediatrics
| 2022
von
Singh, K.
|
Puri, R.
|
Bijarnia-Mahay, S.
| +7
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7
Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India
enthalten in:
Indian pediatrics
| 2022
von
Singh, K.
|
Puri, R.
|
Bijarnia-Mahay, S.
| +7
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8
Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India
enthalten in:
Indian pediatrics
| 2022
von
Singh, K.
|
Puri, R.
|
Bijarnia-Mahay, S.
| +7
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9
Transformative effect of a Humanitarian Program for individuals affected by rare diseases : building support systems and creating local expertise
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Verma, I.
|
El-Beshlawy, A.
|
Tylki-Szymańska, A.
| +7
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10
Transformative effect of a Humanitarian Program for individuals affected by rare diseases: building support systems and creating local expertise
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Verma, I.
|
El-Beshlawy, A.
|
Tylki-Szymańska, A.
| +7
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Medienart
395
Aufsätze
304
Gedruckte Aufsätze
91
E-Artikel
91
E-Ressourcen
Zeitschriftentitel
158
Indian journal of pediatrics
60
Indian pediatrics
40
The Indian journal of medical research
8
Human genetics
8
Indian journal of medical research
7
Journal of fetal medicine
5
American journal of medical genetics
5
Clinical genetics
4
Bulletin of the World Health Organization
4
The Southeast Asian journal of tropical medicin...
3
Community genetics
3
Human mutation
3
Lancet (London, England)
3
Orphanet journal of rare diseases
3
The journal of obstetrics and gynecology of India
2
Acta neurologica Scandinavica
2
American journal of hematology
2
Birth defects original article series
2
Folia biologica
2
Hypertension in pregnancy
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Thema
266
Journal Article
53
Case Reports
45
Research Support, Non-U.S. Gov't
18
Comparative Study
15
Review
12
Editorial
9
Codon
9
Letter
7
India
7
Microarray
7
alpha-Fetoproteins
5
Klinische Studie
5
Lysosomal storage disorders
5
Microdeletions
4
9004-22-2
4
Asia
4
Biology
4
Biomarkers
4
CNV
4
Comment
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Erscheinungszeitraum
68
2000-
183
1900-1999
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Sprache
367
Englisch
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