| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00247-017-3821-1 |
| P698 | PubMed publication ID | 28303321 |
| P50 | author | Mai-Lan Ho | Q87834045 |
| P2093 | author name string | Orit A Glenn | |
| Jonathan B Strober | |||
| Eliott H Sherr | |||
| P2860 | cites work | Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan | Q24321692 |
| Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan | Q28249364 | ||
| Magnetic resonance imaging of the fetal brain and spine: an increasingly important tool in prenatal diagnosis, part 1. | Q31060966 | ||
| B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations | Q37711819 | ||
| Abnormal development of the human cerebral cortex. | Q37803421 | ||
| Differential diagnosis of ventriculomegaly and brainstem kinking on fetal MRI. | Q40899546 | ||
| Neuroimaging manifestations and classification of congenital muscular dystrophies. | Q46018845 | ||
| Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies | Q48666364 | ||
| P433 | issue | 7 | |
| P921 | main subject | dystroglycanopathy | Q29014918 |
| P304 | page(s) | 884-888 | |
| P577 | publication date | 2017-03-16 | |
| P1433 | published in | Pediatric Radiology | Q7159214 |
| P1476 | title | Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation | |
| P478 | volume | 47 |
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