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Publications by Inessa Grinberg

Molecular and Neuroimaging Findings in Pontocerebellar Hypoplasia Type 2 (PCH2): Is Prenatal Diagnosis Possible?

American Journal of Medical Genetics, Part A
Genetics
2010English

Reciprocal Fusion Transcripts of Two Novel Zn-Finger Genes in a Female With Absence of the Corpus Callosum, Ocular Colobomas and a Balanced Translocation Between Chromosomes 2p24 and 9q32

European Journal of Human Genetics
Genetics
2003English

Related publications

Pontocerebellar Hypoplasia Type 2

2020English

Pontocerebellar Hypoplasia Type 4

2020English

Pontocerebellar Hypoplasia Type 5

2020English

Pontocerebellar Hypoplasia Type 8

2020English

Pontocerebellar Hypoplasia Type 6

2020English

Natural Course of Pontocerebellar Hypoplasia Type 2A

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2014English

Non-Syndromic Pontocerebellar Hypoplasia

2020English

P95 the Undeclared New Type of Pontocerebellar Hypoplasia

2019English

LMOD3 -Associated Nemaline Myopathy: Prenatal Ultrasonographic, Pathologic, and Molecular Findings

Journal of Ultrasound in Medicine
Nuclear MedicineRadiologyUltrasound TechnologyRadiologicalImagingMedicine
2018English

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