| P2093 | author name string | R T Bronson | |
| | K R Johnson | |
| | M T Davisson | |
| | L R Donahue | |
| | S A Cook | |
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| | SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12 | Q28236737 |
| | Chromosomal mapping in the mouse of eight K(+)-channel genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal | Q28237187 |
| | Growth hormone deficiency in 'little' mice results in aberrant body composition, reduced insulin-like growth factor-I and insulin-like growth factor-binding protein-3 (IGFBP-3), but does not affect IGFBP-2, -1 or -4 | Q28508126 |
| | A genetic map of the mouse suitable for typing intraspecific crosses | Q33959542 |
| | A newly recognized dwarfing syndrome. | Q34705475 |
| | A Macintosh program for storage and analysis of experimental genetic mapping data | Q36763737 |
| | Megalencephaly: definition and classification | Q39641245 |
| | Megalencephaly: types, clinical syndromes, and management | Q39706397 |
| | Quantitative trait loci associated with brain weight in the BXD/Ty recombinant inbred mouse strains | Q41109484 |
| | Heritable aspects of anomalous myelinated fibre tracts in the forebrain of the laboratory mouse | Q41513542 |
| | Unilateral megalencephaly with nerve cell hypertrophy. An anatomical and quantitative histochemical study | Q42443643 |
| | Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome | Q47234247 |
| | Genetic and phenotypic variation in weight of brain and spinal cord between inbred strains of mice | Q47363318 |
| | Insulin-like growth factor I increases brain growth and central nervous system myelination in transgenic mice | Q48313440 |
| | Megalencephaly in children: Clinical syndromes, genetic patterns, and differential diagnosis from other causes of megalocephaly | Q48761312 |
| | Cerebral spongy degeneration of infancy. A biochemical and ultrastructural study of affected twins | Q48800755 |
| | Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. | Q51362516 |
| | Sotos syndrome--autosomal dominant inheritance substantiated. | Q52081914 |
| | Macrocephaly with head growth parallel to normal growth pattern: neurological, developmental, and computerized tomography findings in full-term infants. | Q52297602 |
| | A simple, rapid, and sensitive DNA assay procedure | Q56879279 |
| | Growth enhancement of transgenic mice expressing human insulin-like growth factor I | Q67979226 |
| | Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations | Q70807877 |
| | Children with large heads: a practical approach to diagnosis in 557 children, with special reference to 109 children with megalencephaly | Q70907253 |
| | Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse | Q72586237 |
| P433 | issue | 12 | |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 871-876 | |
| P577 | publication date | 1996-12-01 | |
| P1433 | published in | Mammalian Genome | Q1348949 |
| P1476 | title | Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain | |
| P478 | volume | 7 | |