Secondary Logo

Journal Logo

January 2008 - Volume 17 - Issue 1
pp: 1-78

Screening for subtelomeric chromosome alteration in a consecutive series of newborns with congenital defects

Rodríguez, Laura; Martínez-Fernández, María Luisa; Mansilla, Elena; More

Clinical Dysmorphology. 17(1):5-12, January 2008.

Expanding the phenotype of 22q11 deletion syndrome: the MURCS association

Uliana, Vera; Giordano, Nicola; Caselli, Rossella; More

Clinical Dysmorphology. 17(1):13-17, January 2008.

De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment

Kosho, Tomoki; Sakazume, Satoru; Kawame, Hiroshi; More

Clinical Dysmorphology. 17(1):31-34, January 2008.