Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jacqueline Carroll"'
Publikováno v:
Clinical and Experimental Ophthalmology. 31:392-396
Background: Retinoblastoma is the most common malignant ocular tumour of childhood. It results from mutations in the retinoblastoma gene, RB1, which may be sporadic or heritable. Only 10−25% of patients have a family history of retinoblastoma and c
Publikováno v:
Clinicalexperimental ophthalmology. 31(5)
Retinoblastoma is the most common malignant ocular tumour of childhood. It results from mutations in the retinoblastoma gene, RB1, which may be sporadic or heritable. Only 10-25% of patients have a family history of retinoblastoma and can be assumed
Autor:
Hamish S. Scott, Graeme Suthers, Lesley Rawlings, Catherine Carmichael, Meryl Altree, Ella J Wilkins, William N. Patton, Jacqueline Carroll
Publikováno v:
Blood. 110:4244-4244
Aim To identify the causative heritable mutation in a family with autosomal dominant familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML). Method Confirmation of family pedigree, enrolment into ethics committee approved
Publikováno v:
Journal of Clinical Psychology. 40:410-413
Fourteen patients diagnosed as borderline on the basis of the Diagnostic Interview for Borderlines obtained a mean group profile of 8-2-7 similar in configuration, but more elevated than that obtained by a group of 7 diagnostically heterogeneous cont
Publikováno v:
The Journal of nervous and mental disease. 170(8)
As part of a larger study of pathological self-injury, 14 self-mutilators and 14 psychiatric controls matched for age, sex, and inpatient/outpatient status were administered the Diagnostic Interview for Borderlines. Consistent with Gunderson's theory
Publikováno v:
The American journal of psychiatry. 137(7)
Publikováno v:
American Journal of Psychiatry. 138:855-b