Splitting and lumping in the nosology of XLMR
- 1 January 2000
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 97 (3) , 174-182
- https://doi.org/10.1002/1096-8628(200023)97:3<174::aid-ajmg1034>3.0.co;2-4
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Breakthroughs in molecular andcellular mechanisms underlying X-linked mental retardationHuman Molecular Genetics, 1999
- Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitorHuman Molecular Genetics, 1998
- Mind the GAP, Rho, Rab and GDINature Genetics, 1998
- Mutations in GDI1 are responsible for X-linked non-specific mental retardationNature Genetics, 1998
- New X‐linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardationAmerican Journal of Medical Genetics, 1994
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: A new X‐linked mental retardation syndromeAmerican Journal of Medical Genetics, 1988
- Linkage analysis suggests at least two loci for X‐linked nonspecific mental retardationAmerican Journal of Medical Genetics, 1988
- The MASA syndrome: A new heritable mental retardation syndromeClinical Genetics, 1974
- HEREDITARY STENOSIS OF THE AQUEDUCT OF SYLVIUS AS A CAUSE OF CONGENITAL HYDROCEPHALUSBrain, 1949