C R Schad

Author PubWeight™ 6.28^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Fluorescence in situ hybridization with X and Y chromosome probes for cytogenetic studies on bone marrow cells after opposite sex transplantation.	Bone Marrow Transplant	1993	1.05
2	Structure and chromosome localization of the human eosinophil-derived neurotoxin and eosinophil cationic protein genes: evidence for intronless coding sequences in the ribonuclease gene superfamily.	Genomics	1990	1.01
3	The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALL.	Cancer Genet Cytogenet	1993	0.95
4	Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.	Clin Genet	1996	0.92
5	Frequency and photographs of HGM11 chromosome anomalies in bone marrow samples from 3,996 patients with malignant hematologic neoplasms.	Cancer Genet Cytogenet	1993	0.82
6	Detection of RB1 deletions by fluorescence in situ hybridization in malignant hematologic disorders.	Cancer Genet Cytogenet	1998	0.79
7	Fluorescent in situ hybridization studies of lymphocytes and neutrophils in chronic granulocytic leukemia.	Cancer Genet Cytogenet	1995	0.76
8	Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocations.	Mayo Clin Proc	1992	0.75
9	Cytogenetic and molecular genetic methods for diagnosis and treatment response in chronic granulocytic leukemia.	Cancer Genet Cytogenet	1997	0.75