Published in Hum Genet on April 07, 1977
A new method for the analysis of cohort studies: implications of the multistage theory of carcinogenesis applied to occupational arsenic exposure. Environ Health Perspect (1983) 1.33
Chromosomal methods in population studies. Environ Health Perspect (1981) 1.07
Arsenic elevates the sister chromatid exchange (SCE) rate in human lymphocytes in vitro. Arch Dermatol Res (1980) 0.85
Biomonitoring exposure to metal compounds with carcinogenic properties. Environ Health Perspect (1993) 0.82
Effects of coal combustion products and metal compounds on sister chromatid exchange (SCE) in a macrophagelike cell line. Environ Health Perspect (1983) 0.79
Normal sister chromatid exchange in lymphocytes from patients with multiple epidermal cancer? Arch Dermatol Res (1987) 0.79
Investigation of the sister chromatid exchange (SCE) frequency in one patient with xeroderma pigmentosum. Arch Dermatol Res (1981) 0.75
The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations. Am J Hum Genet (1967) 2.32
A human chondrodysplasia due to a mutation in a TGF-beta superfamily member. Nat Genet (1996) 2.11
Concordance between telepathologic diagnosis and conventional histopathologic diagnosis: a multiobserver store-and-forward study on 20 skin specimens. Arch Dermatol (2002) 2.07
Cutaneous osteomas: a clinical and histopathologic review. Arch Dermatol Res (1977) 1.95
Successful bone-marrow transplantation for infantile malignant osteopetrosis. N Engl J Med (1980) 1.95
Classification and birth prevalence of orofacial clefts. Am J Med Genet (1998) 1.83
Cutaneous manifestations of Crohn's disease. J Am Acad Dermatol (1981) 1.82
Robin's syndrome. A probably X-linked recessive subvariety exhibiting persistence of left superior vena cava and atrial septal defect. Am J Dis Child (1970) 1.76
Popliteal pterygium syndrome . A syndrome comprising cleft lip-palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics (1968) 1.62
Coliphages as ecological indicators of enteroviruses in various water systems. Bull World Health Organ (1981) 1.55
Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet (1982) 1.45
Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid--a syndrome. Cancer (1968) 1.41
Leprosy type 1 reaction as the first manifestation of borderline lepromatous leprosy in a young native German. Br J Dermatol (1997) 1.39
Malformation syndromes. A selected miscellany. Birth Defects Orig Artic Ser (1975) 1.35
Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia. Pediatrics (1981) 1.27
Granulomatous perivasculitis in Crohn's disease. Arch Dermatol (1981) 1.19
Down syndrome due to partial trisomy 21q. Clin Genet (1977) 1.18
Cell line derived from a metastasis of a human testicular germ cell tumor. Cancer Res (1980) 1.10
Seckel's dwarfism: analysis of chromosome breakage and sister chromatid exchanges. Am J Dis Child (1979) 1.07
Facial clefting and its syndromes. Birth Defects Orig Artic Ser (1971) 1.06
Human genotoxicity: pesticide applicators and phosphine. Science (1989) 1.03
Muir-Torre syndrome - treatment with isotretinoin and interferon alpha-2a can prevent tumour development. Dermatology (2000) 1.01
Cranio-carpo-tarsal dysplasia or the whistling face syndrome. II. Oral intercommissural distance in children. Am J Dis Child (1969) 0.97
Characterization of a cell line from human transitional cell cancer of the urinary tract. J Natl Cancer Inst (1974) 0.97
Prevalence o f malocclusion in Chippewa Indian children. J Dent Res (1968) 0.96
Chromosome rearrangements in fumigant appliers: possible relationship to non-Hodgkin's lymphoma risk. Cancer Epidemiol Biomarkers Prev (1993) 0.94
A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type. Hum Genet (1989) 0.94
Albinism in Nigeria with delineation of new recessive oculocutaneous type. Clin Genet (1980) 0.91
Cytogenetic differentiation of Fanconi anemia, "idiopathic" aplastic anemia, and Fanconi anemia heterozygotes. Am J Med Genet (1983) 0.91
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study. Am J Dermatopathol (1999) 0.90
Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block. Hum Genet (1980) 0.90
Studies on the transformation of rat embryo cells of low passage by carcinogenic fluorenylhydroxamic acids and their acetate esters. In Vitro (1978) 0.90
Taurodontism: an anomaly of teeth reflecting disruptive developmental homeostasis. Am J Med Genet Suppl (1988) 0.89
[Heredity of fistulas of the lower lip and their relation to cleft lip and palate]. Cesk Pediatr (1966) 0.89
Chromosomes and spray adhesivess. N Engl J Med (1974) 0.88
Sister chromatid exchange in dyskeratosis congenita lymphocytes. J Med Genet (1977) 0.88
[Congenital dysplasia of the musculi pectorales associated with congenital hand and finger malformations of the ipsilateral upper limb]. Acta Chir Orthop Traumatol Cech (1966) 0.87
Sister chromatid exchange in lymphocytes from patients with malignant lymphoma. Hum Genet (1978) 0.86
[Congenital, plaque-like osteoma of the skin in an infant]. Hautarzt (1978) 0.86
Trisomy 22 with 'cat eye' anomaly. J Med Genet (1977) 0.85
Interstitial deletion of 10q: clinical features and literature review. Am J Med Genet (1992) 0.85
Synthesis of unsaturated carnitine esters with N-acyl imidazoles. J Lipid Res (1982) 0.84
Prevalence of nosocomial infections in selected hospitals. J Hyg Epidemiol Microbiol Immunol (1987) 0.83
Partial trisomy 4q syndrome: case report and review. Hum Genet (1976) 0.81
Craniocarpotarsal dysplasia or whistling face syndrome. Arch Otolaryngol (1970) 0.81
Psychotropic drugs and ovarial cycle alterations. Act Nerv Super (Praha) (1974) 0.80
DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics. Hum Genet (1984) 0.80
Appearance of the rat testicular receptor for calcitriol (1,25-dihydroxyvitamin D3) during development. J Steroid Biochem (1985) 0.80
Bullous pyoderma gangrenosum. J Am Acad Dermatol (1993) 0.80
Chromosomal breaks in T and B lymphocytes in Fanconi's anemia. Clin Genet (1976) 0.80
Mutagenic activity of anticancer agent cis-dichlorodiammine platinum-II. Mutat Res (1979) 0.80
Atypical cutaneous lymphoproliferative disorder resembling mycosis fungoides in AIDS. Report of a case with concurrent Kaposi's sarcoma. Am J Dermatopathol (1989) 0.80
Familial leukemia and inherited chromosomal aberration. Int J Cancer (1977) 0.79
Mobile encapsulated bodies comprising fat necrosis and fibrous tissue in the abdominal cavity of cows. J Comp Pathol (2010) 0.79
Fluorescing structures of human metaphase chromosomes. Detection of "Y body". Am J Hum Genet (1971) 0.79
Properties of cell lines established from transitional cell cancers of the human urinary tract. Cancer Res (1977) 0.79
"Newer" facial clefting syndromes. Birth Defects Orig Artic Ser (1977) 0.78
Solitary congenital indeterminate cell histiocytoma. Arch Dermatol (1993) 0.78
Syndromes of facial clefting. Scand J Plast Reconstr Surg (1974) 0.78
Fixation of spinal reflexes in rats by central and peripheral sensory input. J Comp Physiol Psychol (1981) 0.78
Sister chromatid exchange in patients with viral disease. Exp Cell Res (1978) 0.78
Delineation of 13q-deletion by replication banding in retinoblastoma. Cytogenet Cell Genet (1981) 0.77
Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques. Cancer Genet Cytogenet (1982) 0.77
Surface charge effects in protein adsorption on nanodiamonds. Nanoscale (2015) 0.77
Contrasting renal haemodynamic responses to the angiotensin converting enzyme inhibitor enalapril and the beta-adrenergic antagonist metoprolol in essential hypertension. J Hypertens Suppl (1984) 0.76
Central and peripheral influences on retention of postural asymmetry in rats. J Comp Physiol Psychol (1982) 0.76
Effects of fosenopril, a once-daily angiotensin-converting enzyme inhibitor, on resting and exercise-induced changes of blood pressure, hormonal variables, and plasma potassium in essential hypertension. Am J Hypertens (1988) 0.76
Prevention of health damage caused by agrochemical substances. Czech Med (1982) 0.76
Ring chromosome 14 and immunoglobulin locus. Am J Med Genet (1984) 0.76
Effect of sodium fluoride on growth of human diploid cells in culture. Pharmacol Toxicol (1990) 0.76
Sweet syndrome: vasculitis or not? Br J Dermatol (2006) 0.76
No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome. Am J Med Genet (1982) 0.76
Chromosome breaks and sister chromatid exchanges in albinos in Nigeria. Clin Genet (1979) 0.76
Results of screening for phenylalanine and other amino acid disturbances among pregnant women. J Inherit Metab Dis (1980) 0.75
[Pregnancy hyperphenylalanemia and its diagnostic importance (author's transl)]. Cas Lek Cesk (1975) 0.75
[Maternal hyperphenylalaninemia and intrauterine damage to the CNS]. Cesk Neurol Neurochir (1974) 0.75
[Preparation of polyacrylamide gel containing hormones for the depot administration in vivo]. Cesk Farm (1972) 0.75
[Some genetic problems in women with late toxemia--study of genealogy]. Cesk Gynekol (1967) 0.75
[Prenatal diagnosis of the carrier of the translocation form of Down's disease]. Cesk Gynekol (1972) 0.75
[Neonatal hormonal responses of baby girls from pregnancies followed up by ultrasound. Investigation to verify the safety of repeated ultrasonic examinations (author's transl)]. Cesk Gynekol (1973) 0.75
A new method for studying the influence of steroids on the vaginal cells of the trigone of the rat. Acta Cytol (1972) 0.75
[Personal experiences with Minitrol]. Cesk Gynekol (1973) 0.75
[Our experiences with cytodiagnosis of prolonged pregnancy]. Cesk Gynekol (1969) 0.75
Health aspects of Danube river floods. Ann Soc Belg Med Trop (1976) 0.75
[Use of primary fluorescence in hormonal cytology]. Cesk Gynekol (1973) 0.75
[Results of perinatal prevention in pregnancies based on records of the genetic clinic in 1970]. Cesk Gynekol (1972) 0.75
[Genetic aspects of planned parenthood]. Cesk Gynekol (1972) 0.75
[Labor induction in suspected prolonged pregnancy]. Cesk Gynekol (1969) 0.75
Structural basis of banding pattern of human chromosomes. Cytogenet Cell Genet (1973) 0.75
Cleft uvula: a microform of facial clefts and its genetic basis. Birth Defects Orig Artic Ser (1971) 0.75
Seasonal incidence of cleft lip and palate in Czech regions. Cleft Palate J (1969) 0.75
[Perinatal genetic counseling]. Zentralbl Gynakol (1972) 0.75
[Economic aspects of virus hepatitis]. Bratisl Lek Listy (1969) 0.75
Prenatal sex determination. Detection of "Y body". Obstet Gynecol (1971) 0.75
[Prenatal determination of child's sex]. Cesk Gynekol (1972) 0.75
[Results of chromosomal examinations of lymphocyte cultures from cord blood of infants from pregnancies followed-up by ultrasound (author's transl)]. Cesk Gynekol (1973) 0.75