In vitro growth and chromosome constitution of placental cells. II. Hydatidiform moles.

PubWeight™: 0.78‹?›

🔗 View Article (PMID 3979121)

Published in Cytogenet Cell Genet on January 01, 1985

Authors

P A Hunt, P A Jacobs

Articles by these authors

Segmental aneuploidy and the genetic gross structure of the Drosophila genome. Genetics (1972) 22.68

Trisomy in man. Annu Rev Genet (1984) 4.15

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome. Cell (1991) 3.98

A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet (1980) 3.82

A cytogenetic survey of 11,680 newborn infants. Ann Hum Genet (1974) 3.80

Further segregation analysis of the fragile X syndrome with special reference to transmitting males. Hum Genet (1985) 3.42

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature (1997) 3.27

The marker (X) syndrome: a cytogenetic and genetic analysis. Ann Hum Genet (1984) 3.17

Aggressive behavior, mental sub-normality and the XYY male. Nature (1965) 3.10

Trisomy 21: association between reduced recombination and nondisjunction. Am J Hum Genet (1991) 3.08

Correlation between euploid structural chromosome rearrangements and mental subnormality in humans. Nature (1974) 2.23

An analysis of the break points of structural rearrangements in man. J Med Genet (1974) 2.18

Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice. J Cell Biol (1999) 2.08

Fragile X premutation screening in women with premature ovarian failure. Hum Reprod (1998) 1.99

Structural abnormalities of the Y chromosome in man. Nature (1966) 1.99

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21. Am J Hum Genet (1981) 1.97

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes. J Med Genet (2005) 1.94

X-linked mental retardation: a study of 7 families. Am J Med Genet (1980) 1.93

Chromosome studies on randomly chosen men and women. Lancet (1965) 1.92

Incidence and mutation rates of structural rearrangements of the autosomes in man. Ann Hum Genet (1972) 1.86

Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole. Ann Hum Genet (1982) 1.86

Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol (1997) 1.85

Chromosome studies on 3500 newborn male infants. Lancet (1970) 1.82

Segregation of genetic markers in families with chromosome polymorphisms and structural rearrangements involving chromosome 1. Ann Hum Genet (1974) 1.81

Direct analysis of the chromosome constitution of human spermatozoa. Nature (1978) 1.76

Mutation rates of structural chromosome rearrangements in man. Am J Hum Genet (1981) 1.74

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities. Clin Genet (1972) 1.70

The inheritance of translocations in man: data from families ascertained through a balanced heterozygote. Ann Hum Genet (1970) 1.66

An imprinted gene(s) for diabetes? Nat Genet (1995) 1.65

Mechanism of origin of complete hydatidiform moles. Nature (1980) 1.55

Acrocentric chromosome associations in man. Am J Hum Genet (1976) 1.53

Three patients with ring (X) chromosomes and a severe phenotype. J Med Genet (1993) 1.52

Structural abnormalities of the sex chromosomes. Br Med Bull (1969) 1.51

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet (1991) 1.47

Cytogenetic and molecular studies of trisomy 13. J Med Genet (1987) 1.43

The mouse Y* chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region. Cytogenet Cell Genet (1991) 1.39

Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation. Hum Reprod (2002) 1.38

Pericentric inversion of a group C autosome: a study of three families. Ann Hum Genet (1968) 1.37

A centromere map of the X chromosome from trisomies of maternal origin. Ann Hum Genet (1990) 1.37

Origin of human trisomics and polyploids. Hum Hered (1977) 1.34

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers. Proc Natl Acad Sci U S A (1986) 1.34

The chromosome complement of human gametes. Oxf Rev Reprod Biol (1992) 1.34

A survey of sex chromatin abnormalities in mental hospitals. J Med Genet (1968) 1.32

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation. Hum Mol Genet (1994) 1.32

Nonrandom segregation of the mouse univalent X chromosome: evidence of spindle-mediated meiotic drive. Genetics (2000) 1.31

Epidemiology of chromosome abnormalities in man. Am J Epidemiol (1977) 1.30

More on marker X chromosomes, mental retardation and macro-orchidism. N Engl J Med (1979) 1.30

An inherited X-autosome translocation in man. Ann Hum Genet (1971) 1.30

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. Hum Mol Genet (1996) 1.27

The origin of human triploids. Ann Hum Genet (1978) 1.27

X chromosome loss and ageing. Cytogenet Genome Res (2007) 1.26

Translocation heterozygosity and associated subfertility in man. Cytogenetics (1972) 1.25

Probable assignment of the alpha locus of haptoglobin to chromome 16 in man. Nature (1969) 1.25

Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet (1995) 1.23

A cytogenetic study of spontaneous abortions in Hawaii. Ann Hum Genet (1978) 1.23

X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Hum Mol Genet (1996) 1.23

Sex-chromosome pairing and activity during mammalian meiosis. Bioessays (1992) 1.20

A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities. Clin Genet (1978) 1.18

Trisomy in humans: incidence, origin and etiology. Curr Opin Genet Dev (1993) 1.18

Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation. Dev Biol (1999) 1.16

C- and Q-band polymorphisms in the chromosomes of three human populations. Ann Hum Genet (1976) 1.16

The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results. Clin Genet (1975) 1.16

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. Hum Mol Genet (1996) 1.13

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns. Hum Genet (1994) 1.13

Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype. Am J Med Genet (1992) 1.11

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors. Hum Mol Genet (2001) 1.11

Cross-cultural differences in GPs' attitudes towards complementary and alternative medicine: a survey comparing regions of the UK and Germany. Complement Ther Med (2002) 1.11

Expression of the marker (X) (q28) in lymphoblastoid cell lines. Am J Hum Genet (1982) 1.11

Mortality and cancer incidence in persons with numerical sex chromosome abnormalities: a cohort study. Ann Hum Genet (2001) 1.10

The origin of the extra Y chromosome in males with a 47,XYY karyotype. Hum Mol Genet (1999) 1.09

The parental origin of the extra X chromosome in 47,XXX females. Am J Hum Genet (1990) 1.09

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity. Am J Hum Genet (2003) 1.08

A study of females with deletions of the short arm of the X chromosome. Hum Genet (1998) 1.07

Intellectual deficits after transient tyrosinemia in the term neonate. Pediatrics (1976) 1.07

Human chromosome heteromorphisms (variants). Prog Med Genet (1977) 1.07

A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man. J Med Genet (1992) 1.06

Coordinating the segregation of sister chromatids during the first meiotic division: evidence for sexual dimorphism. J Cell Sci (2001) 1.06

Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes. Proc Natl Acad Sci U S A (1993) 1.06

Maternal age in trisomy. Ann Hum Genet (1988) 1.05

Cytogenetic studies of chromosome aberrations. Hum Genet (1990) 1.05

The use of cells doubly labelled with [14C]inositol and [3H]inositol to search for a hormone-sensitive inositol lipid pool with atypically rapid metabolic turnover. J Endocrinol (1989) 1.04

Marker X syndrome in an oriental family with probable transmission by a normal male. Am J Med Genet (1982) 1.04

Aging and aneuploidy: evidence for the preferential involvement of the inactive X chromosome. Cytogenet Cell Genet (1985) 1.03

Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment. Neuropsychologia (2000) 1.03

Fragile X premutations in familial premature ovarian failure. Lancet (1995) 1.03

The interrelationships of the inositol phosphates formed in vasopressin-stimulated WRK-1 rat mammary tumour cells. Biochem J (1992) 1.02

Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone. Hum Mol Genet (2001) 1.02

Cytogenetic and molecular studies of Down syndrome individuals with leukemia. Am J Hum Genet (1995) 1.01

The incidence and etiology of sex chromosome abnormalities in man. Birth Defects Orig Artic Ser (1979) 1.00

A common intracellular allosteric binding site for antagonists of the CXCR2 receptor. Br J Pharmacol (2010) 0.99

Lateral asymmetry in human constitutive heterochromatin. Chromosoma (1975) 0.99

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis. Genet Res (1991) 0.99

Chromosome mutations: frequency at birth in humans. Humangenetik (1972) 0.99

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'. J Med Genet (1992) 0.98

Meiotic aneuploidy in the XXY mouse: evidence that a compromised testicular environment increases the incidence of meiotic errors. Hum Reprod (1999) 0.98

Molecular studies of the parental origin and nature of human X isochromosomes. Cytogenet Cell Genet (1988) 0.97

Further information on the identity of 47,XYY males. Br Med J (1968) 0.97

Inositol lipids: receptor-stimulated hydrolysis and cellular lipid pools. Philos Trans R Soc Lond B Biol Sci (1988) 0.95