Published in Clin Genet on April 01, 1985
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype. J Med Genet (1993) 1.14
Interstitial deletion and ring chromosome derived from 16q. J Med Genet (1987) 0.92
Association of a de novo 16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes. BMC Med Genet (2009) 0.81
Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis. J Med Genet (1987) 0.80
Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism. Eur J Hum Genet (2010) 0.76
Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements. Mol Cytogenet (2016) 0.75
Hepatocellular carcinoma and hepatitis B virus. A prospective study of 22 707 men in Taiwan. Lancet (1981) 13.54
Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma. Proc Natl Acad Sci U S A (1983) 7.01
Genetic disorders in children and young adults: a population study. Am J Hum Genet (1988) 4.98
Piracetam therapy does not enhance cognitive functioning in children with down syndrome. Arch Pediatr Adolesc Med (2001) 2.72
Age- and gender-related differences in clinical productivity among Canadian pediatricians. Pediatrics (1990) 2.70
Pediatric manpower in Canada: a cross-country survey. CMAJ (1989) 2.61
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum Mol Genet (2001) 2.48
Incidence of inborn errors of metabolism in British Columbia, 1969-1996. Pediatrics (2000) 2.40
Unstable spiral modes in disk-shaped galaxies. Proc Natl Acad Sci U S A (1976) 2.30
GTP hydrolysis by arf-1 mediates sorting and concentration of Golgi resident enzymes into functional COP I vesicles. EMBO J (1999) 2.30
Efficacy of hepatitis B immune globulin for prevention of perinatal transmission of the hepatitis B virus carrier state: final report of a randomized double-blind, placebo-controlled trial. Hepatology (1983) 2.22
The chromosome constitution of 1000 human spermatozoa. Hum Genet (1983) 2.21
Life expectancy of patients with newly-diagnosed HIV infection in the era of highly active antiretroviral therapy. QJM (2007) 2.21
Congenital anomalies in American Indians of British Columbia. Genet Epidemiol (1986) 2.13
Radial loops and helical coils coexist in metaphase chromosomes. Cell (1985) 2.09
Errors of morphogenesis: concepts and terms. Recommendations of an international working group. J Pediatr (1982) 2.04
The British Columbia Registry for Handicapped Children and Adults: evolutionary changes over twenty years. Can J Public Health (1975) 2.00
Human centromeric DNAs. Hum Genet (1997) 1.94
cGMP-elevating agents suppress proliferation of vascular smooth muscle cells by inhibiting the activation of epidermal growth factor signaling pathway. Circulation (1997) 1.93
Down syndrome in British Columbia, 1952-73: incidence and mean maternal age. Teratology (1976) 1.89
Progressive hemifacial atrophy (Parry-Romberg syndrome) report with review of genetics and nosology. Am J Med Genet (1983) 1.83
Incidence of hepatitis B virus infections in preschool children in Taiwan. J Infect Dis (1982) 1.74
Outbreak of paralytic poliomyelitis, Taiwan. Lancet (1984) 1.68
Hepatitis B virus markers in Chinese twins. Anticancer Res (1989) 1.68
Pharmacokinetics of SCH 56592, a new azole broad-spectrum antifungal agent, in mice, rats, rabbits, dogs, and cynomolgus monkeys. Antimicrob Agents Chemother (2000) 1.64
Pediatric medication errors: predicting and preventing tenfold disasters. J Clin Pharmacol (1994) 1.62
Chromosome 6q deletions: a report of two additional cases and a review of the literature. Am J Med Genet (1990) 1.62
Aberrant expression of an amplified c-myb oncogene in two cell lines from a colon carcinoma. Proc Natl Acad Sci U S A (1984) 1.59
Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: a new syndrome. J Pediatr (1971) 1.56
Denture stomatitis--a review of the aetiology, diagnosis and management. Aust Dent J (1992) 1.55
Exogenous adenosine 3': 5'-monophosphate can release yeast from catabolite repression. Biochem Biophys Res Commun (1978) 1.53
Inheritance of tuberous sclerosis. Lancet (1979) 1.52
Pleomorphic adenoma with extensive necrosis: report of two cases. Oral Dis (2004) 1.51
HEDJ, an Hsp40 co-chaperone localized to the endoplasmic reticulum of human cells. J Biol Chem (2000) 1.50
Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet (1972) 1.48
Isolation of functional Golgi-derived vesicles with a possible role in retrograde transport. J Cell Biol (1998) 1.45
Borderline normal intelligence in the Smith-Lemli-Opitz (RSH) syndrome. Am J Med Genet (1980) 1.45
Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1. Eur J Hum Genet (2001) 1.44
Anodontia of permanent teeth (OMIM # 206780) and pegged/missing maxillary lateral incisors (OMIM # 150400) in the same family. Am J Med Genet (2000) 1.43
Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement. Clin Genet (1986) 1.42
Endolymphatic sac ballooning surgery for Menière's disease. Ann Otol Rhinol Laryngol (1994) 1.41
Serial changes of serum interleukin-6, interleukin-8, and tumor necrosis factor alpha among patients with Kawasaki disease. J Pediatr (1992) 1.40
Selective loss of antigen-specific Ir gene function in IA mutant B6.C-H-2bm12 is an antigen presenting cell defect. Proc Natl Acad Sci U S A (1981) 1.40
Absorption of subcutaneous injection of Tc-99m pertechnetate via acupuncture points and non-acupuncture points. Am J Chin Med (1994) 1.40
Care provided to Madeleine. CMAJ (1996) 1.39
Progressive cerebellar ataxia associated with Hand-Schüller-Christian disease. Dev Med Child Neurol (1971) 1.38
Primary oral squamous cell carcinoma: an analysis of 703 cases in southern Taiwan. Oral Oncol (1999) 1.35
Purification and properties of a nicotinamide adenine dinucleotide-linked dehydrogenase that serves an Escherichia coli mutant for glycerol catabolism. J Bacteriol (1979) 1.35
Relative frequency of the Hurler and Hunter syndromes. N Engl J Med (1971) 1.35
Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique. Hum Genet (1976) 1.33
Effects of inhibition of nitric oxide formation on basal vasomotion and endothelium-dependent responses of the coronary arteries in awake dogs. J Clin Invest (1991) 1.32
Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndrome. Hum Genet (1979) 1.31
Ring formation of chromosomes nos. 19 and 20. Cytogenetics (1972) 1.30
The incidence of congenital malformations in a Chinese population: the Taipei collaborative study. Teratology (1972) 1.30
Impact of thrombocytopenia on survival of baboons with genetically modified pig liver transplants: clinical relevance. Am J Transplant (2009) 1.29
NADP + -specific isocitrate dehydrogenase of Escherichia coli. I. Purification and characterization. Biochim Biophys Acta (1972) 1.29
Radical scavenger and antihepatotoxic activity of Ganoderma formosanum, Ganoderma lucidum and Ganoderma neo-japonicum. J Ethnopharmacol (1995) 1.28
Incidence rates for cleft lip and palate in British Columbia 1952-71 for North American Indian, Japanese, Chinese and total populations: secular trends over twenty years. Teratology (1977) 1.28
Poland syndrome in British Columbia: incidence and reproductive experience of affected persons. Am J Med Genet (1977) 1.27
Comparative studies on aetiology and epidemiology of viral conjunctivitis in three countries of East Asia--Japan, Taiwan and South Korea. Int J Epidemiol (1987) 1.26
Subtle immunologic abnormalities in four boys with subacute sclerosing panencephalitis. N Engl J Med (1971) 1.26
Myxoid tumor of the oral cavity with features of superficial angiomyxoma: report of a case. J Oral Maxillofac Surg (1998) 1.26
Antioxidant and free radical scavenging effects of baicalein, baicalin and wogonin. Anticancer Res (2000) 1.24
Nitric oxide modulates epicardial coronary basal vasomotor tone in awake dogs. Am J Physiol (1990) 1.24
Changing trends of prostate cancer in Asia. Aging Male (2004) 1.24
Genitourinary anomalies are a component manifestation in the ectodermal dysplasia, ectrodactyly, cleft lip/palate (EEC) syndrome. Am J Med Genet (1988) 1.24
Anti-inflammatory effects of emodin from ventilago leiocarpa. Am J Chin Med (1996) 1.23
Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome. Am J Med Genet (1983) 1.21
[The campomelic syndrome]. Presse Med (1971) 1.21
Carcinosarcoma of the renal pelvis: a case report with immunohistochemical study. Changgeng Yi Xue Za Zhi (1996) 1.20
Antiviral activity of Plantago major extracts and related compounds in vitro. Antiviral Res (2002) 1.20
[Clinical experience of laryngeal mask airway in lateral position during anesthesia]. Acta Anaesthesiol Sin (1995) 1.19
Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome. Am J Med Genet (1988) 1.18
Trisomy of the short arm of chromosome 17. Humangenetik (1974) 1.16
Micrognathia, polydactyly, and cleft palate. J Pediatr (1968) 1.15
Molecular events during the release of delta-aminolevulinate dehydratase from catabolite repression. J Bacteriol (1978) 1.14
Trisomy 9 mosaicism with multiple congenital anomalies. J Med Genet (1973) 1.13
Discrete spiral modes in disk galaxies: Some numerical examples based on density wave theory. Proc Natl Acad Sci U S A (1977) 1.13
Regulation of steroidogenic acute regulatory protein expression and progesterone production in endometriotic stromal cells. J Clin Endocrinol Metab (2001) 1.13
A new familial syndrome with ataxia, hearing loss, and mental retardation. Report of three brothers. Arch Neurol (1973) 1.13
Tentative assignment of piebald trait gene to chromosome band 4q12. Hum Genet (1986) 1.13
Comparing whole body (18)F-2-deoxyglucose positron emission tomography and technetium-99m methylene diphosphonate bone scan to detect bone metastases in patients with breast cancer. J Cancer Res Clin Oncol (2002) 1.12
Incidence and inheritance of the 1/29 and 14/20 Robertsonian translocations in Canadian beef cattle. Genome (1987) 1.12
Classification of perinatal deaths: development of the Australian and New Zealand classifications. J Paediatr Child Health (2004) 1.11
Retrospective study on nasopharyngeal carcinoma. J Natl Cancer Inst (1973) 1.11
In vitro antiviral activities of Caesalpinia pulcherrima and its related flavonoids. J Antimicrob Chemother (2003) 1.11
Renal abnormalities in the Russell-Silver syndrome. Pediatrics (1973) 1.11
Antimicrobial activity of honokiol and magnolol isolated from Magnolia officinalis. Phytother Res (2001) 1.10
[9-14C]Fluorene hydroperoxide as a possible intermediate in the hydroxylation of [9-14C]fluorene by rat liver homogenate. Biochim Biophys Acta (1969) 1.10
Incidence and genetics of Legg-Perthes disease (osteochondritis deformans) in British Columbia: evidence of polygenic determination. J Med Genet (1972) 1.10
Antitumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic mice. Cancer Res (1998) 1.10
The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12. Ann Genet (1985) 1.09
Low prevalence of rheumatoid arthritis in Chinese. Prevalence survey in a rural community. J Rheumatol Suppl (1983) 1.08
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana. Am J Med Genet (1985) 1.08
Schizotypy in community samples: the three-factor structure and correlation with sustained attention. J Abnorm Psychol (1997) 1.08
Application of FTA sample collection and DNA purification system on the determination of CTG trinucleotide repeat size by PCR-based Southern blotting. J Clin Lab Anal (1999) 1.08
Conservation of human gamma-X centromeric satellite DNA among primates with an autosomal localization in certain Old World monkeys. Chromosome Res (1999) 1.08
Hypospadias in successive generations - possible dominant gene inheritance. Clin Genet (1976) 1.08