Published in Can Fam Physician on April 01, 1988
Genetics in pediatrics. Can Fam Physician (1988) 0.88
Use of phosphate and vitamin D to prevent dwarfism and rickets in X-linked hypophosphatemia. N Engl J Med (1972) 1.46
Invasive prenatal testing. Can Fam Physician (1988) 1.24
Genetic family history questionnaire. J Med Genet (1978) 1.21
Why I shall stay in rural practice. Can Fam Physician (1987) 1.17
Von Hippel-Lindau disease in a Newfoundland kindred. CMAJ (1986) 1.08
The genogram. J Fam Pract (1980) 1.07
Von Hippel-Lindau's disease: a report of five cases. Can Med Assoc J (1969) 1.02
Problems in genetics: getting help. Can Fam Physician (1988) 1.00
Support services in genetics. Can Fam Physician (1988) 0.99
Introduction to DNA-Based Genetic Diagnostics. Can Fam Physician (1988) 0.87
Multifactorial inheritance in man. Can Fam Physician (1988) 0.82
The "new genetics": an ethical perspective from family practice. Can Fam Physician (1988) 0.82
Basic cytogenetics for office practice. Can Fam Physician (1988) 0.81
Mendelian genetics. Can Fam Physician (1988) 0.81
Transforming Theory into Preventive Genetics in rural Communities. Can Fam Physician (1987) 0.81
The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N Engl J Med (1989) 4.41
Reduced fertility and postischaemic brain injury in mice deficient in cytosolic phospholipase A2. Nature (1997) 3.70
Identification of the mouse karyotype by quinacrine fluorescence, and tentative assignment of seven linkage groups. Proc Natl Acad Sci U S A (1971) 3.10
A novel member of the RING finger family, KRIP-1, associates with the KRAB-A transcriptional repressor domain of zinc finger proteins. Proc Natl Acad Sci U S A (1996) 2.54
The Krüppel-associated box-A (KRAB-A) domain of zinc finger proteins mediates transcriptional repression. Proc Natl Acad Sci U S A (1994) 2.46
The 13q-deletion syndrome. Am J Hum Genet (1969) 2.06
Delayed profound respiratory depression after premedication with trimeprazine. Anaesthesia (1992) 2.02
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21). Am J Hum Genet (1975) 1.87
Identification of translocation chromosomes by quinacrine fluorescence. Am J Dis Child (1972) 1.62
Quinacrine fluorescent karyotypes of human diploid and heteroploid cell lines. Cytogenetics (1971) 1.54
Angioscopic evaluation of site-specific administration of ReoPro. Cathet Cardiovasc Diagn (1997) 1.49
Kid-1, a putative renal transcription factor: regulation during ontogeny and in response to ischemia and toxic injury. Mol Cell Biol (1993) 1.44
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers). Proc Natl Acad Sci U S A (1972) 1.42
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cells. Science (1971) 1.37
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence. Humangenetik (1971) 1.28
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-). J Pediatr (1970) 1.25
Recruiting participants for community-based research: the Diabetic Retinopathy Awareness Program. Ann Epidemiol (2000) 1.23
Duplication 9q34 syndrome. Am J Hum Genet (1983) 1.22
TRIP-Br: a novel family of PHD zinc finger- and bromodomain-interacting proteins that regulate the transcriptional activity of E2F-1/DP-1. EMBO J (2001) 1.22
Method for locating the centromeres of mouse meiotic chromosomes and its application to T163H and T70H translocations. Exp Cell Res (1972) 1.19
Deletion of cytosolic phospholipase A(2) suppresses Apc(Min)-induced tumorigenesis. Proc Natl Acad Sci U S A (2001) 1.17
Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity. Hum Genet (1983) 1.15
Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype. Am J Med Genet (1998) 1.15
Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. Am J Hum Genet (1986) 1.14
The 9p- syndrome. Ann Genet (1976) 1.12
Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients. J Pediatr (1970) 1.11
Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence. J Cell Sci (1973) 1.03
PLIP, a novel splice variant of Tip60, interacts with group IV cytosolic phospholipase A(2), induces apoptosis, and potentiates prostaglandin production. Mol Cell Biol (2001) 1.01
Short- and long-term association between uric acid and a natural disaster. Psychosom Med (1997) 0.97
Renal concentrating defect in mice lacking group IV cytosolic phospholipase A(2). Am J Physiol Renal Physiol (2001) 0.95
Quinacrine fluorescence patterns of human D group chromosomes. Nature (1971) 0.94
Accessibility of intensive care facilities in Ireland to critically ill patients. Ir Med J (2002) 0.91
Spreading of inactivation in an (X;14) translocation. Am J Med Genet (1978) 0.91
Expression of the transcriptional repressor protein Kid-1 leads to the disintegration of the nucleolus. J Biol Chem (1999) 0.89
Human chromosomes in 18 man-mouse somatic hybrid cell lines analysed by quinacrine fluorescence. J Cell Sci (1973) 0.89
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter. Arch Dermatol (1985) 0.87
Modelling the demographics of the Irish cattle population. Prev Vet Med (2009) 0.86
A mammalian expression vector for the expression of GAL4 fusion proteins with an epitope tag and histidine tail. Anal Biochem (1994) 0.85
Detection of angiographically significant coronary artery disease with accelerated intermittent imaging after intravenous administration of ultrasound contrast material. Am Heart J (2000) 0.84
Pectoralis major defect and Poland sequence in second cousins: extension of the Poland sequence spectrum. Am J Med Genet (1989) 0.82
Distinctive fluorescence of quinacrine-labelled human G group chromosomes. Nat New Biol (1971) 0.82
Detection of minute deletions in human karyotypes. Cytogenetics (1969) 0.82
Transforming Theory into Preventive Genetics in rural Communities. Can Fam Physician (1987) 0.81
Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse. Genetics (1972) 0.80
A simple technique for recording and counting sweat pores on the dermal ridges. Clin Genet (1986) 0.79
Efficiency of Dispatch and Infiltrator cardiac infusion catheters in arterial localization of nanoparticles in a porcine coronary model of restenosis. J Drug Target (2002) 0.79
Chromosomal heterogeneity in the RAG and MSWBS mouse tumor cell lines. Cancer Res (1974) 0.78
9pter leads p22 deletion syndrome: a case report. Birth Defects Orig Artic Ser (1976) 0.78
The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs. Nucleic Acids Res (1991) 0.78
Real-time perfusion echocardiography during treadmill exercise and dobutamine stress testing. Heart (2009) 0.78
Novel technique for coil embolization of intercostal branch of internal mammary artery graft. Cathet Cardiovasc Diagn (1997) 0.77
Two-stage liver resection and chemotherapy for bilobar colorectal liver metastases. Eur J Surg Oncol (2004) 0.77
A new method for automatic tracking of facial landmarks in 3D motion captured images (4D). Int J Oral Maxillofac Surg (2012) 0.76
Effects of SP500263, a novel selective estrogen receptor modulator, on bone, uterus, and serum cholesterol in the ovariectomized rat. Calcif Tissue Int (2003) 0.76
Reversible dysfunction of T-lymphocytes in common variable immunodeficiency. Can Med Assoc J (1977) 0.75
HaeIII RFLP for salivary proline-rich protein gene probe (pPRPII2.2RP). Nucleic Acids Res (1991) 0.75
Assignment of the red cell antigen, Targett (Rh40), to the Rh blood group system. Am J Hum Genet (1979) 0.75
Meiosis in Arthroderma benhamiae (=Trichophyton mentagrophytes). Sabouraudia (1968) 0.75
The KySS (Keep your children/yourself Safe and Secure) campaign: a national effort to reduce psychosocial morbidities in children and adolescents. J Pediatr Health Care (2001) 0.75
Partial deletion of the long arm of chromosome E-18. Pediatrics (1970) 0.75
Sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures. J Clin Dysmorphol (1984) 0.75
A "new" low incidence red cell antigen, NFLD. Hum Genet (1984) 0.75
A study of the chromosomes of the normal male rabbit and two intersex rabbits with quinacrine fluorescence and Giemsa banding. Cytologia (Tokyo) (1974) 0.75
Medical Quality Assurance Programme. Med J Aust (1994) 0.75
Meiotic confirmation of the identification of chromosomes 9 and 13 in T(9 ; 19)163H, T(5 ; 13)264 Ca, and T(1 ; 13)70H stocks in Mus musculus. Chromosoma (1973) 0.75
Adrenocortical disorders. Int Anesthesiol Clin (1997) 0.75
An old injury with a modern twist. Anaesthesia (2000) 0.75
Splenectomy in hairy cell leukaemia. Ir Med J (1987) 0.75
Chromosome numbers in species of Nannizzia and Arthroderma. Mycologia (1970) 0.75
Replication pattern and quinacrine fluorescence of the chromosomes of a CV-1-derived African green monkey cell line. Cytogenet Cell Genet (1973) 0.75
Magnetic field exposure assessment: a comparison of various methods. Bioelectromagnetics (1999) 0.75
Blood groups in Newfoundlanders. Gene Geogr (1991) 0.75