Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome
- 1 February 2002
- Vol. 79 (2) , 186-196
- https://doi.org/10.1006/geno.2002.6695
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- No evidence of dup(7)(p11.2p13) in Silver-Russell syndromeAmerican Journal of Medical Genetics, 2001
- Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndromeEuropean Journal of Human Genetics, 2001
- Reply to Mergenthaler et al.American Journal of Human Genetics, 2001
- A New Subfamily of High Molecular Mass CDC2-Related Kinases with PITAI/VRE MotifsBiochemical and Biophysical Research Communications, 2000
- Cognitive abilities associated with the Silver-Russell syndrome.Archives of Disease in Childhood, 1994
- Dup(lq)(q42→qter) syndrome: Case report and review of literatureAmerican Journal of Medical Genetics, 1993
- Russell-Silver syndrome and Wilms tumorThe Journal of Pediatrics, 1993
- An infant with deletion of the distal long arm of chromosome 15 (q26.1→qter) and loss of insulin‐like growth factor 1 receptor geneAmerican Journal of Medical Genetics, 1991
- Three‐generation dominant transmission of the Silver‐Russell syndromeAmerican Journal of Medical Genetics, 1990
- X‐linked short stature with skin pigmentation: evidence for heterogeneity of the Russell‐Silver syndromeClinical Genetics, 1986