TY  - GEN
AU  - Mansilla, E
AU  - Rodríguez, Luis
AU  - Martinez-Fernandez, Maria Luisa
AU  - Rodríguez de Cía, J
AU  - García Vicent, C
AU  - Martínez-Frías, María Luisa
PY  - 2006
SN  - 0210–3893
UR  - http://hdl.handle.net/20.500.12105/14016
AB  - Monosomy 10p is a rare chromosomal anomaly having quite variable clinical expression, showing in some patients the DiGeorge anomaly. Here we report a malformed newborn, whose high resolution G-band karyotype showed an abnormal short arm of chromosome...
LA  - spa
PB  - Instituto de Salud Carlos III (ISCIII). Instituto de Investigación de Enfermedades Raras (IIER)
TI  - Monosomía parcial 10p en un caso con fenotipo similar al síndrome de Ritscher-Schinzel
T2  - Partial monosomy 10p in a case with a phenotype resembling Ritscher-Schinzel syndrome
TY  - research article
ER  -