HUM-MOLGEN DIAGnostics/Clinical Research

July, 12 1999

I've had a request for information of similar cases from a mother of a 3 year old girl with karyotype : 46,XX,del(7)(pter->q22.3::q31.1->qter) de novo. This mother seeks addresses of families or support groups of rare chromosome abnormalities, in the hope that families with children with similar deletion breakpoints might be able to communicate.

Many thanks.

Kerry Fagan ,
Chief Cytogeneticist
HAPS,   Newcastle Mater Hospital
Waratah   NSW   2398  AUSTRALIA
tel: +61 249 211246        fax: +61 249 211248