Published in Cytogenetics on January 01, 1968
Cytogenetic analysis of pseudolinkage of ldh Loci in the teleost genus salvelinus. Genetics (1973) 1.92
Fertility in balanced heterozygotes for a familial centric fusion translocation, t(DgDg). J Med Genet (1971) 1.03
Cytogenetic studies in a patient with a de novo t(Cq-;Gp+). J Med Genet (1970) 1.01
A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome. J Med Genet (1970) 0.98
Tertiary trisomy in a human kindred containing an E/G translocation. Am J Hum Genet (1971) 0.88
Three generations and seven family members with a t(21q22q) chromosome. J Med Genet (1974) 0.80
The telomeric sync model of speciation: species-wide telomere erosion triggers cycles of transposon-mediated genomic rearrangements, which underlie the saltatory appearance of nonadaptive characters. Naturwissenschaften (2014) 0.79
Inherited t(13q14q) in two retarded sisters. Am J Hum Genet (1972) 0.78
Report of large kinship with familial translocation between chromosomes 21 and 22. Can Med Assoc J (1977) 0.75
Three generations and six family members with a t(13q15q) chromosome. J Med Genet (1973) 0.75
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin Genet (1975) 3.81
Down syndrome and recent demographic trends in Manitoba. J Med Genet (1978) 2.34
Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively. Somat Cell Mol Genet (1987) 2.21
Prenatal diagnosis of genetic disease in Canada: report of a collaborative study. Can Med Assoc J (1976) 2.07
Chorionic villus sampling and amniocentesis for prenatal diagnosis. Lancet (1997) 2.04
Familial mental retardation in a family with an inherited chromosome rearrangement. J Med Genet (1974) 1.57
Regional localization of 18 human X-linked DNA sequences. Cytogenet Cell Genet (1986) 1.48
Localization of the gene encoding human factor V to chromosome 1q21-25. Genomics (1988) 1.46
Chromosome studies in a neonatal population. Can Med Assoc J (1972) 1.42
The characteristics of a population of Canadian women offered maternal serum alphafetoprotein screening during pregnancy. Can J Public Health (1986) 1.39
Chromosomal mosaicism in diagnostic amniotic fluid cell cultures. Pediatr Res (1974) 1.34
Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. Chromosoma (1986) 1.33
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor. Somat Cell Mol Genet (1985) 1.24
Report of the committee on the genetic constitution of chromosome 1. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet (1982) 1.16
Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR. Am J Med Genet (1990) 1.16
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
Genetic intersexuality in goats. J Reprod Fertil Suppl (1969) 1.10
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. Am J Hum Genet (1987) 1.08
A DNA marker for human chromosome 8 that detects alleles of differing sizes. Cytogenet Cell Genet (1986) 1.08
Human population cytogenetics: dilemmas and problems. Am J Hum Genet (1976) 1.07
A summary of the human gene map, 1973-1977. Cytogenet Cell Genet (1978) 0.96
Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet (1979) 0.96
A 48, XXXX female. J Med Genet (1974) 0.94
Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Final report. Prenat Diagn (1992) 0.93
Chromosome findings in chronic psychotic patients. Br J Psychiatry (1968) 0.93
Proceedings: Report of the Committee on the Genetic Constitution of Chromosome 1. Cytogenet Cell Genet (1974) 0.92
Significance of sex chromosome derived heterochromatin in mammals. Nature (1968) 0.92
Report of the committee on the genetic constitution of chromosomes 1 and 2. Birth Defects Orig Artic Ser (1976) 0.91
Non-random X chromosome expression in female mules and hinnies. Nature (1971) 0.91
Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids. Am J Hum Genet (1975) 0.91
Non-random inactivation of the X chromosome in the female mule. Nature (1970) 0.91
Cytogenetic disorders. N Engl J Med (1984) 0.89
The association of glucose phasphate isomerase expression with human chromosome 19 using somatic cell hybrids. Cytogenet Cell Genet (1973) 0.88
Mapping the human 5S RNA genes on chromosome 1 using translocations. Cytogenet Cell Genet (1975) 0.86
G6PD expression and X chromosome late replication in fibroblast clones from a female mule. Nature (1972) 0.86
A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies. Birth Defects Orig Artic Ser (1982) 0.86
Non-random x-inactivation in the female mule. Nature (1969) 0.86
Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants. Birth Defects Orig Artic Ser (1986) 0.86
Deletion of the short arm of chromosome No. 10. J Med Genet (1975) 0.85
Detection and cross-reaction of H-Y antigen by haemagglutination. J Immunogenet (1978) 0.85
Cytogenetic and endocrine studies of a freemartin heifer and its bull co-twin. Cytogenetics (1969) 0.85
Homozygous Robertsonian translocations in a fetus with 44 chromosomes. Hum Genet (1982) 0.85
Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells. Proc Natl Acad Sci U S A (1973) 0.84
Non-random late replication of X chromosomes in mules and hinnies. Nature (1971) 0.84
Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21-qter) region of chromosome 18 in man. Cytogenet Cell Genet (1975) 0.83
C-Band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population. Hum Genet (1979) 0.83
Report of the Committee on the Genetic Constitution of Chromosome 1. Cytogenet Cell Genet (1984) 0.82
Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study. Can Med Assoc J (1979) 0.81
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy. Clin Genet (1978) 0.81
Analyses of data on rates of cytogenetic disorders in live births. Am J Hum Genet (1978) 0.81
The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7. Somat Cell Mol Genet (1989) 0.80
Structural gene encoding human factor XII is located at 5q33-qter. Somat Cell Mol Genet (1988) 0.80
Fetal sex. Lancet (1970) 0.80
Characteristics of an HPRT-deficient chinese hamster cell line. Cytogenet Cell Genet (1974) 0.80
An intersex goat with a bilaterally asymmetrical reproductive tract. J Reprod Fertil (1968) 0.80
Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter leads to q21. Biochem Genet (1980) 0.79
Proceedings: Localization of the structural gene for human peptidase-A to chromosome 18. Cytogenet Cell Genet (1974) 0.79
The gene for clotting factor 10 is mapped to 13q32----qter. Cytogenet Cell Genet (1986) 0.78
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site. Nature (1983) 0.78
The H-Y antigen:production of antibodies, detection, and cross-reaction between mouse, rat, and human. Cytogenet Cell Genet (1978) 0.78
Chromosomal localization and structure of the human P1 protamine gene. Genomics (1989) 0.78
Ethical considerations in newborn chromosome screening programs. Birth Defects Orig Artic Ser (1979) 0.78
Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis. Nature (1982) 0.77
Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophy. J Neurol Sci (1983) 0.77
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome. Hum Genet (1991) 0.77
Heterogeneity in the biochemical characteristics of red blood cell hypoxanthine-guanine phosphoribosyl transferase from two unrelated patients with the Lesch-Nyhan syndrome. Biochem Genet (1973) 0.77
Proceedings: Synteny of the IDH-1 and MDH-1 gene loci in man and probable assignment to chromosome 2. Cytogenet Cell Genet (1974) 0.76
Banding patterns of metaphase chromosomes in Down's syndrome. Lancet (1971) 0.76
Evidence for the role of the maternal immune system in balancing the sex ratio in mice. J Reprod Immunol (1980) 0.76
Tertiary trisomy 14: is there a syndrome? Birth Defects Orig Artic Ser (1976) 0.75
Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1. Genomics (1988) 0.75
Limb defects and chorionic villus sampling. Lancet (1996) 0.75
The William Allan Memorial Award. Presented to Patricia A. Jacobs, D.Sc., at the annual meeting of the American Society of Human Genetics, Dallas, October 28-31, 1981. Am J Hum Genet (1982) 0.75
Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7. Nucleic Acids Res (1987) 0.75
A BglII RFLP at the human prolactin gene locus on chromosome 6 (PRL). Nucleic Acids Res (1991) 0.75
TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7. Nucleic Acids Res (1989) 0.75
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease. Pediatr Res (1978) 0.75
Regional localizations of four markers on chromosome 1 using a 1/4 translocation. Cytogenet Cell Genet (1976) 0.75
Assignment of three human gene loci to regions of chromosome 2. Birth Defects Orig Artic Ser (1975) 0.75
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons. Am J Med Genet (1992) 0.75
Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man. Cytogenet Cell Genet (1975) 0.75
Proposed banding nomenclature for the Chinese hamster chromosomes (Cricetulus grises). Birth Defects Orig Artic Ser (1976) 0.75
Assignment of the inorganic chromosome 10 in man. Birth Defects Orig Artic Ser (1976) 0.75
Prenatal diagnosis in Canada--1990: a review. Prenat Diagn (1994) 0.75
Mapping the human 5S RNA genes on chromosome 1 using translocations. Birth Defects Orig Artic Ser (1975) 0.75
Assignment of three human gene loci to regions of chromsome 2. Cytogenet Cell Genet (1975) 0.75
Standardization in human cytogenetics. Cytogenet Cell Genet (1975) 0.75
Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication. Somat Cell Mol Genet (1993) 0.75
Localization of gene loci on chromosome 12 and the X in man. Birth Defects Orig Artic Ser (1975) 0.75
Assignment of the inorganic pyrophosphatase gene locus (PP) to chromosome 10 in man. Cytogenet Cell Genet (1976) 0.75
A cytogenetic survey of 14,069 new born infants. II. Preliminary clinical findings on children with sex chromosome anomalies. Clin Genet (1976) 0.75
Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. Birth Defects Orig Artic Ser (1976) 0.75
The human complement after trypsin pretreatment as compared to the Paris standard. Humangenetik (1975) 0.75
Further data on the assignment of the phosphoglucomutase (PGM2) gene locus to chromosome 4 in man. Birth Defects Orig Artic Ser (1975) 0.75
Localization of gene loci on chromosome 12 and the X in man. Cytogenet Cell Genet (1975) 0.75
Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. Cytogenet Cell Genet (1976) 0.75
Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21 leads to qter) region of chromosome 18 in man. Birth Defects Orig Artic Ser (1975) 0.75
Regional localization of four markers on chromosome 1 using 1/4 translocation. Birth Defects Orig Artic Ser (1976) 0.75