Published in Clin Genet on July 01, 1979
First trimester fetal karyotyping in twin pregnancy. J Med Genet (1984) 0.81
Antenatal diagnosis of Niemann-Pick disease in a twin pregnancy. J Med Genet (1981) 0.75
Genetic amniocentesis in twin pregnancies. Br Med J (1979) 0.75
Novel beta-lactamase in a clinical isolate of Klebsiella pneumoniae conferring unusual resistance to beta-lactam antibiotics. J Antimicrob Chemother (1987) 3.45
Down syndrome and recent demographic trends in Manitoba. J Med Genet (1978) 2.34
Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothers. Am J Med Genet (1978) 2.27
Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization. Fertil Steril (1995) 1.93
A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve. J Am Coll Cardiol (1997) 1.88
Renal tubular dysgenesis: a not uncommon autosomal recessive syndrome: a review. Am J Med Genet (1992) 1.63
VACTERL with hydrocephalus: further delineation of the syndrome(s) Am J Med Genet (1989) 1.55
Black grandmothers in multigenerational households: diversity in family structure and parenting involvement in the Woodlawn community. Child Dev (1990) 1.55
Phenotypic correlations in patients with ring chromosome 22. Clin Genet (1977) 1.54
Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33. Clin Genet (1982) 1.49
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21. Am J Med Genet (1992) 1.46
A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center. Clin Genet (2000) 1.44
Post-translational control of the MEF2A transcriptional regulatory protein. Nucleic Acids Res (1999) 1.37
Chromosomal mosaicism in diagnostic amniotic fluid cell cultures. Pediatr Res (1974) 1.34
Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. Teratology (1977) 1.33
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). Teratology (1976) 1.33
Ethical aspects of dementia research: informed consent and proxy consent. Clin Res (1994) 1.26
A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus. Genomics (1989) 1.24
C60La: a deflated soccer ball? J Am Chem Soc (1986) 1.20
Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission. Science (1993) 1.20
Neural tube defects in Eastern Ontario and Western Quebec: demography and family data. Am J Med Genet (1984) 1.19
The Coffin-Lowry syndrome. Experience from four centres. Clin Genet (1982) 1.18
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families. Am J Med Genet (1996) 1.18
Implications of malformations not due to amniotic bands in the amniotic band sequence. Am J Med Genet (1986) 1.11
A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations. Cytogenet Cell Genet (1978) 1.11
Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population. Am J Hum Genet (1989) 1.10
Chromosomal nondisjunction: the action of colcemid on Chinese hamster cells in vitro. Cytogenetics (1969) 1.09
Sweeteners, dyes, and other excipients in vitamin and mineral preparations. Clin Pediatr (Phila) (1996) 1.09
An epidemiological study of facial clefting in Manitoba. J Med Genet (1980) 1.07
Growth and development in thanatophoric dysplasia. Am J Med Genet (1989) 1.07
The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome. Clin Genet (1985) 1.03
COFS syndrome revisited. Birth Defects Orig Artic Ser (1978) 1.00
Geroderma osteodysplastica. A report of two affected families. Hum Genet (1978) 0.97
Duchenne's muscular dystrophy: studies in cultured fibroblasts. Lancet (1977) 0.96
Trigonocephaly and associated minor anomalies in mother and son. J Med Genet (1976) 0.95
The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformities. Am J Med Genet (1979) 0.94
VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Am J Med Genet (1993) 0.94
Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Am J Med Genet (1993) 0.94
An outbreak of S typhimurium in sheep and its consequences. Vet Rec (1976) 0.93
Low rate of adequate folic acid supplementation in well-educated women of high socioeconomic status attending a genetics clinic. CMAJ (2001) 0.92
APC I1307K increases risk of transition from polyp to colorectal carcinoma in Ashkenazi Jews. Gastroenterology (2001) 0.92
Mosaic tetrasomy 21 in a liveborn male infant. Clin Genet (1982) 0.92
Is there a fetal gasoline syndrome? Teratology (1979) 0.90
Toxocara in the mouse: a model for parasite-altered host behaviour? J Helminthol (2001) 0.90
Colostral constituents including immunoglobulins in the first three milkings postpartum. J Dairy Sci (1978) 0.89
Apparent Smith-Lemli-Opitz syndrome in a child with a previously undescribed form of mucolipidosis not involving the neurons. Am J Med Genet (1990) 0.89
Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagen. Hum Genet (1986) 0.89
Distribution of Boophilus species ticks in Swaziland. Trop Anim Health Prod (1991) 0.88
A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome. J Med Genet (2004) 0.88
Absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy: an autosomal recessive oculo-renal-cerebellar syndrome. Am J Med Genet (1982) 0.88
Characterization and isolation of a sperm-coating antigen from rabbit seminal plasma with capacity to block fertilization. J Reprod Fertil (1969) 0.88
Proteolytic activities of human Campylobacter pylori and ferret gastric Campylobacter-like organism. Biochem Biophys Res Commun (1989) 0.87
A familial interstitial deletion of the long arm of chromosome 21. Clin Genet (1990) 0.87
Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and Tay-Sachs patients and amniotic fluid cells. Clin Genet (1973) 0.87
Inversion of chromosome 2 (p11p13): frequency and implications for genetic counselling. Hum Genet (1985) 0.87
Effects of diet and time on blood serum proteins in the newborn calf. J Dairy Sci (1970) 0.87
The in vitro isolation and characterization of monosomic sublines derived from a Colcemid-treated Chinese hamster cell population. Cytogenet Cell Genet (1976) 0.87
Hepatic fibrosis, polycystic kidney, colobomata and encephalopathy in siblings. Clin Genet (1974) 0.86
Generalization from single sentence to multisentence production in severely aphasic patients. Brain Lang (1997) 0.86
A quantitative analysis of colcemid-induced chromosomal nondisjunction in Chinese hamster cells in vitro. Cytogenet Cell Genet (1973) 0.86
Seminal antigens: their alteration in the genital tract of female rabbits and during partial in vitro capacitation with beta amylase and beta glucuronidase. Biol Reprod (1972) 0.86
Interstitial deletion of the long arm of chromosome 10. Ann Genet (1980) 0.85
Inheritance of branchial sinuses and preauricular fistulae. Teratology (1974) 0.85
AvaII RFLP at the human apolipoprotein CII (APO CII) gene locus. Nucleic Acids Res (1987) 0.85
A study of institutionalized mentally retarded patients in Manitoba. I: Classification and preventability. Dev Med Child Neurol (1980) 0.84
Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group. Am J Hum Genet (1995) 0.84
Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles. J Med Genet (2000) 0.83
Midtrimester genetic amniocentesis in eastern Ontario: a review from 1970 to 1985. J Med Genet (1987) 0.83
An interstitial deletion of the long arm of chromosome 13. Clin Genet (1989) 0.82
Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes. Am J Med Genet (1997) 0.82
Characteristic craniofacial appearance and brachytelephalangy in a mother and son with Kallman syndrome in the son. Am J Med Genet (1986) 0.82
Deletion and uniparental disomy involving the same maternal chromosome 15. N Engl J Med (1994) 0.82
Linkage relationships of X-linked choroideremia to DXYS1 and DXS3. Hum Genet (1987) 0.82
Sex chromosome mosaicism not detected at amniocentesis. Prenat Diagn (1990) 0.82
Grandmother involvement in child caregiving in an urban community. Gerontologist (1997) 0.82
Why patients do not attend for their appointments at a genetics clinic. J Med Genet (2000) 0.81
Detection at amniocentesis of a maternally inherited X;Y translocation. Clin Genet (1985) 0.81
9qh+ variant band in two families. Am J Med Genet (1992) 0.81
Partial trisomy 8 mosaicism with 46,XX/46,XX-8,+dic(8). Ann Genet (1980) 0.81
Remediating production of tense morphology improves verb retrieval in chronic aphasia. Brain Lang (1997) 0.81
Basic cytogenetics for office practice. Can Fam Physician (1988) 0.81
Acromesomelic dwarfism: description of a patient and comparison with previously reported cases. Hum Genet (1976) 0.81
Family structure and aggressive behavior in a population of urban elementary school children. J Am Acad Child Adolesc Psychiatry (1994) 0.80
Differentiation of rabbit sperm antigens from those of seminal plasma. J Reprod Fertil (1969) 0.80
Cebocephaly in an infant with trisomy 18. J Med Genet (1977) 0.80
Evaluation of cell viability in chromosomally heterogeneous cell populations. Can J Genet Cytol (1971) 0.80
Aphosphorosis in North Yemen cattle. Trop Anim Health Prod (1982) 0.80
Urine odour in a camel suffering from surra (T. evansi infection). Trop Anim Health Prod (1986) 0.80
Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q14 to 6q16. Clin Genet (1993) 0.79
A supernumerary "G" like chromosome originating from a maternal 13;15 translocation in a nondysmorphic, retarded girl. Clin Genet (1979) 0.79
Degenerative myopathy in housed yearling bulls. Vet Rec (1977) 0.79
Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives. Lancet (1998) 0.79
Rodent vectors of Salmonella. Vet Rec (1976) 0.79
Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples. Prenat Diagn (1992) 0.79
Familial pyloric atresia associated with epidermolysis bullosa. J Pediatr (1978) 0.78
Regional histology and histochemistry of the ductus epididymis in the rhesus monkey (Macaca mulatta). Biol Reprod (1978) 0.78
Tay-Sachs disease: ultrastructural studies on cultured fibroblasts. Pediatr Res (1978) 0.78
A comparison of the efficacy and safety of cefuroxime axetil and augmentin in the treatment of upper respiratory tract infections. Drugs Exp Clin Res (1987) 0.78