Published in Can Med Assoc J on June 24, 1967
Chromosome studies in tumours and leukemia. Can Med Assoc J (1990) 0.75
Primary hypomagnesemia with secondary hypocalcemia in an infant. Pediatrics (1968) 1.66
Multiple congenital defects associated with an abnormal unclassifiable karyotype. J Med Genet (1972) 1.39
Ultrastructure and cytochemistry of Clara cells. Am J Pathol (1971) 1.37
Histopathological changes in Duchenne muscular dystrophy. J Neurol Sci (1969) 1.24
Case reports. Intracerebral schwannoma. Report of a case. J Neurosurg (1966) 1.23
Maturation of postnatal human lung and the idiopathic respiratory distress syndrome. Lab Invest (1966) 1.11
Endocrine cells in rat fetal lungs. Ultrastructural and histochemical study. Lab Invest (1974) 1.11
A ring-4 chromosome in a patient with normal intelligence and short stature. J Med Genet (1971) 1.11
Prenatal diagnosis of G M1 -gangliosidosis. N Engl J Med (1973) 1.10
Partial trisomy 4 resulting from a 4-18 reciprocal translocation. Ann Genet (1972) 1.08
Combined mongolism and leukemia. Report of eight cases with chromosome studies. Am J Dis Child (1966) 1.07
The "D" syndrome. Report of four trisomic and one D/D translocation case. Am J Dis Child (1966) 1.06
Change in fiber size in Duchenne muscular dystrophy. Neurology (1967) 1.03
Testicular feminization: a study of two cases, one with a seminoma. Can Med Assoc J (1968) 1.00
Frequency and occurrence of chromosomal syndromes. I. D-Trisomy. Am J Hum Genet (1966) 0.98
Ultrastructure and fluorescence histochemistry of endocrine (APUD-type) cells in tracheal mucosa of human and various animal species. Cell Tissue Res (1975) 0.98
In vitro chromosomal radiosensitivity in "chromosomal breakage syndromes". Cancer (1973) 0.97
Inherited pericentric inversion of a group D (13-15) chromosome. J Med Genet (1972) 0.94
46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3. Clin Genet (1977) 0.93
Frequency and occurrence of chromosomal syndromes: II. E-trisomy. Am J Hum Genet (1966) 0.92
Endocrine-like cells in human fetal lungs: an electron microscopic study. Anat Rec (1972) 0.91
Morphogenesis of human aortic coarctation. Exp Mol Pathol (1967) 0.91
Xanthomatous pseudotumor of lung. A case report with electron microscope and lipid studies. Cancer (1968) 0.90
Nuclear sex identification in human tissues: a histologic study using quinacrine fluorescence. Am J Clin Pathol (1972) 0.85
Double Ph1 chromosomes in chronic granulocytic leukemia. Cancer (1967) 0.85
Rapid Y chromosome identification in human blood smears. Can Med Assoc J (1971) 0.84
Characterization of "free alveolar cells" in experimental adjuvant induced pneumonia. Arch Pathol (1969) 0.83
Double Ph 1 chromosomes in leukaemia. Lancet (1966) 0.83
In vitro chromosomal radiosensitivity in Fanconi's anemia. Blood (1971) 0.82
Fluorescent Y screening of hospitalized newborns. Nature (1971) 0.81
Observations on the relationship of desquamative interstitial pneumonia and pulmonary alveolar proteinosis in childhood: a pathologic and experimental study. Chest (1970) 0.81
Ultrastructural observations on cytodifferentiation of parafollicular cells in the human fetal thyroid. Lab Invest (1971) 0.81
Chromosome studies on cultured tumors of nervous tissue origin. Acta Cytol (1967) 0.80
Lathyrogenic injury to foetal rat aorta and postnatal repair. Exp Mol Pathol (1966) 0.80
Observations on neural spread of herpes simplex virus in suckling mice. An electron microscopic study. Acta Virol (1972) 0.79
Renal function and histology after long-term vitamin D therapy of vitamin D refractory rickets. J Pediatr (1968) 0.78
Comparison of chromosomal behavior in cultured lymphocytes and fibroblasts from patients with chromosomal disorders and controls. Cytogenetics (1971) 0.78
In vitro chromosomal radiosensitivity in patients and in carriers with abnormal non-Down's syndrome karyotypes. Pediatr Res (1972) 0.78
Ultrastructural demonstration of neuronal storage in fetal Tay-Sachs disease. J Neurol Sci (1974) 0.78
Histochemical fibre "types" in Duchenne muscular dystrophy. J Neurol Sci (1970) 0.77
Herpes simplex-hepatitus use of immunoperoxidase to demonstrate the viral antigen in hepatocytes. Gastroenterology (1982) 0.77
18-Trisomy in a 15-year-old girl. Am J Dis Child (1972) 0.76
Chromosome studies in tumours and leukemia. Can Med Assoc J (1990) 0.75
Minute Y chromosome. Ann Genet (1971) 0.75
Males with chronic myeloid leukemia and the 45, XO, Ph1 chromosome pattern. Can Med Assoc J (1974) 0.75
Chromosome abnormalities in patients with syndactyly. Can Med Assoc J (1969) 0.75
Consistent chromosome abnormalities in each of three cases of childhood lymphosarcoma. Eur J Cancer (1972) 0.75
Macrophages and epithelial cells in human amniotic fluid: transmission and scanning electron microscopic study. Am J Anat (1978) 0.75
The effect of postlathyritic medial scar on the progression of experimental atherosclerosis in rats. Exp Mol Pathol (1968) 0.75
Chromosome studies on a radiographer and her family. Report of one case of leukemia and two cases of Down's syndrome. Arch Intern Med (1966) 0.75
Dyeing the Y chromosome. Lancet (1971) 0.75
Early changes in myocardium of rats fed an infarct-producing diet. Arch Pathol (1971) 0.75
Hypodiploid chromosome pattern in acute leukemia following polycythemia vera. Cancer (1967) 0.75
Value of fluorescent Y chromosome and sex chromatin tests. Acta Cytol (1973) 0.75
Familial tertiary trisomy with t (14q-; 1 plus?). Birth Defects Orig Artic Ser (1974) 0.75
Multiple congenital defects associated with 45,XO-46,XYg- mosaicism. Am J Dis Child (1973) 0.75