Published in Lancet on February 12, 1966
Models for clonal evolutions: a study of chronic myelogenous leukemia. Am J Hum Genet (1966) 0.96
Cytogenetic evolution and clonal proliferation in acute transformation of chronic granulocytic leukaemia. Br J Cancer (1968) 0.95
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
Endocrine cells in rat fetal lungs. Ultrastructural and histochemical study. Lab Invest (1974) 1.11
Maturation of postnatal human lung and the idiopathic respiratory distress syndrome. Lab Invest (1966) 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
Morphogenesis of human aortic coarctation. Exp Mol Pathol (1967) 0.91
Endocrine-like cells in human fetal lungs: an electron microscopic study. Anat Rec (1972) 0.91
Xanthomatous pseudotumor of lung. A case report with electron microscope and lipid studies. Cancer (1968) 0.90
Double Ph1 chromosomes in chronic granulocytic leukemia. Cancer (1967) 0.85
Nuclear sex identification in human tissues: a histologic study using quinacrine fluorescence. Am J Clin Pathol (1972) 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
In vitro chromosomal radiosensitivity in Fanconi's anemia. Blood (1971) 0.82
Observations on the relationship of desquamative interstitial pneumonia and pulmonary alveolar proteinosis in childhood: a pathologic and experimental study. Chest (1970) 0.81
Fluorescent Y screening of hospitalized newborns. Nature (1971) 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
Ultrastructural demonstration of neuronal storage in fetal Tay-Sachs disease. J Neurol Sci (1974) 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
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
Clinical conference on leukemia. Chromosome studies in leukemia. Can Med Assoc J (1967) 0.77
18-Trisomy in a 15-year-old girl. Am J Dis Child (1972) 0.76
Chromosome abnormalities in patients with syndactyly. Can Med Assoc J (1969) 0.75
Males with chronic myeloid leukemia and the 45, XO, Ph1 chromosome pattern. Can Med Assoc J (1974) 0.75
Chromosome studies in tumours and leukemia. Can Med Assoc J (1990) 0.75
Minute Y chromosome. Ann Genet (1971) 0.75
Familial tertiary trisomy with t (14q-; 1 plus?). Birth Defects Orig Artic Ser (1974) 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
Consistent chromosome abnormalities in each of three cases of childhood lymphosarcoma. Eur J Cancer (1972) 0.75
The effect of postlathyritic medial scar on the progression of experimental atherosclerosis in rats. Exp Mol Pathol (1968) 0.75
Macrophages and epithelial cells in human amniotic fluid: transmission and scanning electron microscopic study. Am J Anat (1978) 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
Value of fluorescent Y chromosome and sex chromatin tests. Acta Cytol (1973) 0.75
Multiple congenital defects associated with 45,XO-46,XYg- mosaicism. Am J Dis Child (1973) 0.75
Hypodiploid chromosome pattern in acute leukemia following polycythemia vera. Cancer (1967) 0.75