Referencias

1. Preece MA, Abu-Amero SN, Ali Z, et al. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in mUPD7 Silver-Russell syndrome probands. J Med Genet 1999;36:457-60.

2. Bliek J, Terhal P, van den Bogaard MJ, Maas S, Hamel B, Salieb-Beugelaar G, Simon M, et al T, van Smagt J, Kroes H, M. of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRSlike phenotype. Am J Hum Genet. 2006;78:604-14.

3. Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC. The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 1999;36:837–42.

4. A.M. Martínez Nogueiras, M.J. Teixeira Costeira, H.P. Saraiva Moreira y H. Araujo Antunes Síndrome de Russel-Silver.An Esp Pediatr 2001;54:591-4.

5. Eggermann T, Meyer E, Ranke MB, Holder M, Spranger S, Zerres K, Wollmann HA. Diagnostic proceeding in Silver-Russell syndrome. Mol Diagn 2005;9:205-9.

6. Rossignol S. Silver-Russell syndrome and its genetic origins. J Endocrinol Invest 2006;29(Suppl 1):9-10.

7. P Abraham. What is the risk of cancer in a child with hemihypertrophy?. Arch Dis Child 2005;90:1312-3