C. Disteche

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.

A contiguous gene deletion syndrome at 7q21‐q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly

R. Pagon, J. Evans, M. Nuñes, 1994, Clinical dysmorphology.

Deep‐seated, well differentiated lipomatous tumors of the chest wall and extremities

E. Conrad, S. Schuetze, B. Rubin, 2005, Cancer.

The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region

M. Mattei, F. Watrin, C. Mignon, 1997, European journal of human genetics : EJHG.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.