Published in J Med Genet on December 01, 1971
Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies. J Med Genet (1973) 1.36
Inheritance of a ring 14 chromosome. J Med Genet (1981) 1.02
Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm. J Med Genet (1978) 0.84
A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype. J Med Genet (1973) 0.82
Mammalian chromosomes contain cis-acting elements that control replication timing, mitotic condensation, and stability of entire chromosomes. Bioessays (2012) 0.81
Ring chromosomes in human beings. Nature (1962) 1.94
Comparative behavior of ring chromosomes. Am J Hum Genet (1970) 1.87
Chromosome abnormalities in two cases with bilateral radial element defects. J Med Genet (1969) 1.78
Congenital malformations associated with a ring 4 chromosome. J Med Genet (1969) 1.73
Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. Cytogenetics (1966) 1.62
"Cri du Chat" due to a ring-B chromosome. Lancet (1965) 1.54
Ring chromosome 18 in a patient with multiple anomalies. J Med Genet (1967) 1.30
Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients. J Pediatr (1970) 1.11
Short-arm deletion, chromosome 4, (4p-), a syndrome? Ann Hum Genet (1970) 1.03
Primary hypomagnesemia with secondary hypocalcemia in an infant. Pediatrics (1968) 1.66
Clinical and physiological assessment of asthmatic children treated with beclomethasone dipropionate. J Allergy Clin Immunol (1976) 1.59
Psychologic and psychoeducational consequences of thyroxine therapy for juvenile acquired hypothyroidism. J Pediatr (1993) 1.57
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
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
Trisomy 13: a new recurring chromosome abnormality in acute leukemia. Blood (1990) 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
Effect of vasopressin on serum-levels of human growth hormone. Lancet (1967) 1.02
A pituitary abscess simulating an intrasellar tumor. Surg Neurol (1980) 1.01
Testicular feminization: a study of two cases, one with a seminoma. Can Med Assoc J (1968) 1.00
The superior-mesenteric-artery syndrome: cause or complication of anorexia nervosa? Can Psychiatr Assoc J (1978) 0.99
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
Ketoconazole in the management of precocious puberty not responsive to LHRH-analogue therapy. N Engl J Med (1985) 0.96
Growth failure and bony changes induced by deferoxamine. Am J Pediatr Hematol Oncol (1992) 0.94
Inherited pericentric inversion of a group D (13-15) chromosome. J Med Genet (1972) 0.94
Hypothyroidism in cystinosis. A clinical, endocrinologic and histologic study involving sixteen patients with cystinosis. Am J Med (1970) 0.93
46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3. Clin Genet (1977) 0.93
Medical Research Council of Canada therapeutic trial of human growth hormone: first 5 years of therapy. Can Med Assoc J (1975) 0.92
Frequency and occurrence of chromosomal syndromes: II. E-trisomy. Am J Hum Genet (1966) 0.92
Growth, development, and behavioral outcome from mid-adolescence to adulthood in subjects with chromosome aneuploidy: the Toronto Study. Birth Defects Orig Artic Ser (1990) 0.92
Estrogen treatment of girls and constitutional tall stature. Pediatr Clin North Am (1981) 0.91
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
Growth in children with congenital hypothyroidism detected by neonatal screening. J Pediatr (1990) 0.90
Congenital varicella associated with multiple defects. Can Med Assoc J (1973) 0.89
Growth and maturation of patients with Turner's syndrome. Pediatr Res (1983) 0.89
Growth and development from early to midadolescence of children with X and Y chromosome aneuploidy: the Toronto Study. Birth Defects Orig Artic Ser (1986) 0.87
The cerebro-oculo-facio-skeletal syndrome. Clin Genet (1978) 0.86
Bartter's syndrome. A report of four cases, including three in one sibship, with comparative histologic evaluation of the juxtaglomerular apparatuses and glomeruli. Acta Paediatr Scand Suppl (1970) 0.86
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
Brain tumors in children and adolescents--III. Effects of radiation and hormone status on intelligence and on working, associative and serial-order memory. Neuropsychologia (1992) 0.84
Growth and development of children with X and Y chromosome aneuploidy: a prospective study. Birth Defects Orig Artic Ser (1979) 0.83
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
Observations on the relationship of desquamative interstitial pneumonia and pulmonary alveolar proteinosis in childhood: a pathologic and experimental study. Chest (1970) 0.81
Regulation of the androgen receptor by androgen in normal and androgen-resistant genital skin fibroblasts. J Steroid Biochem (1983) 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
Comparison of chromosomal behavior in cultured lymphocytes and fibroblasts from patients with chromosomal disorders and controls. Cytogenetics (1971) 0.78
Ultrastructural demonstration of neuronal storage in fetal Tay-Sachs disease. J Neurol Sci (1974) 0.78
Renal function and histology after long-term vitamin D therapy of vitamin D refractory rickets. J Pediatr (1968) 0.78
Ambiguous genitals in a female infant associated with luteoma of pregnancy. Report of a case. Am J Obstet Gynecol (1968) 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
Growth hormone deficiency in autoimmune polyglandular disease type 1. Saudi Med J (2000) 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
Tenuate dospan as an appetitie suppressant in the treatment of obese children. Appl Ther (1970) 0.76
External genital abnormalities associated with Wilms tumor. Urology (1984) 0.76
Maturation of lung function in children with hypopituitarism. Am Rev Respir Dis (1983) 0.76
Growth and development of children with X and Y chromosome aneuploidy from infancy to pubertal age: the Toronto study. Birth Defects Orig Artic Ser (1982) 0.76
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
Minute Y chromosome. Ann Genet (1971) 0.75
Influence of breast feeding on the clinical features of salt-losing congenital adrenal hyperplasia. Arch Dis Child (1983) 0.75
Chromosome studies in tumours and leukemia. Can Med Assoc J (1990) 0.75
Focal dermal hypoplasia. J Natl Med Assoc (1979) 0.75
Multiple congenital defects associated with 45,XO-46,XYg- mosaicism. Am J Dis Child (1973) 0.75
Consistent chromosome abnormalities in each of three cases of childhood lymphosarcoma. Eur J Cancer (1972) 0.75
Familial persistent müllerian duct syndrome. J Urol (1984) 0.75
Incontinentia pigmenti (Bloch-Sulzberger syndrome). Report of a Negro infant with typical skin lesions, alopecia, and delayed atypical dentition. Clin Pediatr (Phila) (1969) 0.75
Macrophages and epithelial cells in human amniotic fluid: transmission and scanning electron microscopic study. Am J Anat (1978) 0.75
Studies in sickle-cell anemia. XXXI. Preliminary observations on the use of indomethacin in the treatment of thrombotic crises. Med Ann Dist Columbia (1966) 0.75
A report on a family with a (1;2) translocation: cytologic and linkage analysis. Cytogenet Cell Genet (1976) 0.75
Knee fusion after severe injury to the knee joint. J Trauma (1975) 0.75
Management of the teenager with retardation of physical growth or sexual maturation. Pediatr Clin North Am (1974) 0.75
Acute myelomonocytic leukemia (M-4 subtype) with abnormal marrow eosinophilia and a normal chromosome 16. Am J Clin Pathol (1985) 0.75
Selective hypoaldosteronism in infancy. Report of a case. Am J Dis Child (1983) 0.75
Postcraniotomy diabetes insipidus: treatment with DDAVP, a synthetic analog of vasopressin. J Pediatr (1978) 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
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
Humero-radial synostosis. Clin Genet (1978) 0.75
Hypodiploid chromosome pattern in acute leukemia following polycythemia vera. Cancer (1967) 0.75
The effect of postlathyritic medial scar on the progression of experimental atherosclerosis in rats. Exp Mol Pathol (1968) 0.75