Published in Clin Genet on June 01, 1976
Telomere replication, kinetochore organizers, and satellite DNA evolution. Proc Natl Acad Sci U S A (1979) 1.49
Genetic markers on chromosome 7. J Med Genet (1988) 0.95
Constructing agency: the role of language. Front Psychol (2010) 0.89
The "loss" of centromeres from chromosomes of aged women. Am J Hum Genet (1984) 0.87
Distribution of break points in human structural rearrangements. Am J Hum Genet (1983) 0.81
De novo terminal deletion 7p22.1--pter in a child without craniosynostosis. J Med Genet (1989) 0.80
Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages. J Med Genet (1979) 0.78
Cd branding studies in a homologous Robertsonian 13;13 translocation. J Med Genet (1982) 0.78
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature (1998) 3.86
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1). Genomics (1991) 1.99
A human X-Y homologous region encodes "amelogenin". Genomics (1991) 1.66
Prenatal sex determination. Lancet (1990) 1.41
A human Y-chromosome specific repeated DNA family (DYZ1) consists of a tandem array of pentanucleotides. Nucleic Acids Res (1986) 1.34
Restriction fragment length polymorphisms of the human N-myc gene: relationship to gene amplification. Oncogene (1987) 1.22
Sex identification by polymerase chain reaction using X-Y homologous primer. Am J Med Genet (1991) 1.14
A 6p trisomy detected in a family with a "giant satellite". Humangenetik (1975) 1.06
Diagnosis of twin zygosity by hypervariable RFLP markers. Am J Med Genet (1991) 1.01
LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants. Hum Genet (1977) 1.01
Points of exchange in a human no. 5 ring chromosome. Cytogenet Cell Genet (1973) 0.99
A minute deletion of the Y chromosome in men with azoospermia. J Urol (1993) 0.95
Two cases of 8p trisomy in one sibship. Clin Genet (1975) 0.95
Trisomy 10 with mosaicism. A clinical and cytogenetic entity. Jinrui Idengaku Zasshi (1973) 0.95
Evaluation of long-term results of Caroli's disease: 21 years' observation of a family with autosomal "dominant" inheritance, and review of the literature. Hepatogastroenterology (1995) 0.95
Partial tetrasomy 9(9pter to 9q2101) due to an extra iso-dicentric chromosome. Ann Genet (1977) 0.95
High-resolution banding by treating cells with acridine orange before fixation. Cytogenet Cell Genet (1983) 0.95
A case of (13q;18q) translocation with proximal 13q monosomy. Hum Genet (1977) 0.94
Identification of translocated chromosomes by means of autoradiography. Paediatr Univ Tokyo (1967) 0.91
Chondrodysplasia punctata with X;Y translocation. Hum Genet (1988) 0.91
Chromosomal localisation of a Y specific growth gene(s). J Med Genet (1995) 0.91
G-group chromosomes in satellite associations. Cytogenet Cell Genet (1973) 0.90
Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene. Forensic Sci Int (1992) 0.89
A malformed girl with duplication of chromosome 9q. J Med Genet (1984) 0.87
Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome. Ann Neurol (1995) 0.87
The "loss" of centromeres from chromosomes of aged women. Am J Hum Genet (1984) 0.87
Two 47z [DXYS5] RFLPs on the X and the Y chromosome. Nucleic Acids Res (1989) 0.87
Trisomy 9 mosaicism with punctate mineralization in developing cartilages. Eur J Pediatr (1979) 0.86
Amplification of N-myc in a rhabdomyosarcoma. Jpn J Cancer Res (1986) 0.86
Similar chromosomal patterns and lack of N-myc gene amplification in localized and IV-S stage neuroblastomas in infants. Med Pediatr Oncol (1989) 0.85
Dermatoglyphic study of Down's syndrome in Japan. Paediatr Univ Tokyo (1966) 0.85
Down's syndrome: chromosome analysis in 321 cases in Japan. J Med Genet (1969) 0.83
PCR detection of structurally abnormal Y chromosomes. Jpn J Hum Genet (1992) 0.83
A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Hum Mol Genet (1996) 0.83
Fluorescence of Barr body in human amniotic-fluid cells. Lancet (1973) 0.83
A novel nonsense mutation in the HMG box of the SRY gene in a patient with XY sex reversal. Hum Mol Genet (1994) 0.83
Mental retardation and congenital malformations associated with a ring chromosome 9. Hum Genet (1976) 0.83
The loss of centromeric heterochromatin from an inactivated centromere of a dicentric chromosome. Jinrui Idengaku Zasshi (1986) 0.82
High-resolution studies in patients with aniridia-Wilms tumor association. Hum Genet (1985) 0.81
Nonrandom distribution of exchange points in patients with structural rearrangements. Am J Hum Genet (1976) 0.81
DNA replication studies of human D-group chromosomes in satellite associations. Cytogenetics (1969) 0.81
High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities. Hum Genet (1984) 0.81
Distribution of break points in human structural rearrangements. Am J Hum Genet (1983) 0.81
Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb. Am J Hum Genet (1996) 0.80
Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics. J Hum Genet (2001) 0.79
Restriction fragment length polymorphisms of the CYP11B1 gene in the Japanese population. Jpn J Hum Genet (1993) 0.79
Three translocations involving C- or G-group chromosomes. J Med Genet (1973) 0.79
Pitfalls in the use of chromosome variants for paternity dispute cases. Hum Genet (1977) 0.79
Normal Y sequences in Smith-Lemli-Opitz syndrome with total failure of masculinization. Acta Paediatr (1992) 0.78
Detection of engraftment and chimerism after bone marrow transplantation by in situ hybridization using a Y-chromosome specific probe. Am J Hematol (1990) 0.78
The CpG island of the FMR-1 gene is methylated differently among embryonic tissues: implication for prenatal diagnosis. Hum Reprod (1994) 0.78
Sex identification of forensic specimens by polymerase chain reaction (PCR): two alternative methods. Forensic Sci Int (1991) 0.78
11q trisomy detected by fluorescence in situ hybridization. Clin Genet (1993) 0.78
YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31. Genomics (1997) 0.78
Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome. Hum Genet (1982) 0.77
Initiation of DNA replication in human chromosomes. Exp Cell Res (1977) 0.77
Pericentric inversion with a minute deletion of the Y chromosome in a severely oligozoospermic man. Clin Genet (1995) 0.77
CD31 expression on leukocytes is downregulated in vivo during hemodialysis. Nephron (2001) 0.77
Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome. Hum Biol (1999) 0.77
DNA hybridization study using Y-specific probes in an XX-male. Andrologia (1992) 0.77
Interstitial deletion 6q in a malformed boy. Ann Genet (1980) 0.77
Familial cases of Down's syndrome a psu dic (21) (q22) and a rob (14q21q) in cousins. Jinrui Idengaku Zasshi (1981) 0.77
Satellite associations of D group chromosomes in translocation carriers. J Med Genet (1970) 0.77
A presumptive Y-autosome translocation in a boy with congenital malformations. Am J Dis Child (1968) 0.76
Amplified allele of the human N-myc oncogene in neuroblastomas. Jpn J Cancer Res (1988) 0.76
Trisomy of the short arm of chromosome 10. J Med Genet (1975) 0.76
Trisomy/partial monosomy mosaicism of no. 13 pair [46, XX,--13, + rob(13q13q)/46, XX, r(13) (pllq34)]. Jinrui Idengaku Zasshi (1977) 0.76
Inactivation centers in the human X chromosome. Am J Hum Genet (1982) 0.76
Chromosome aberrations and malignant disease among A-bomb survivors. Am J Public Health Nations Health (1970) 0.75
Quinacrine and acridine-R banding without a fluorescence microscope. Hum Genet (1978) 0.75
[Surface anomaly and abnormal dermatoglyphics of Down's syndrome]. Saishin Igaku (1968) 0.75
[Turner's syndrome in pediatrics, with special reference to its chromosome study]. Horumon To Rinsho (1966) 0.75
LBA technique in the detection of chromosome variants. I. Chromosomes with known sites of Q variants. Hum Genet (1977) 0.75
Cytogenetic observations in children with leukemia. Paediatr Univ Tokyo (1970) 0.75
DNA replication studies of human D-group chromosomes in satellite associations. Cytogenetics (1969) 0.75
Chromosomal analysis by mail. Paediatr Univ Tokyo (1968) 0.75
Reply to the letter of Prieto et al. concerning our paper on a case of 13q;18q translocation. Hum Genet (1980) 0.75
[Crying cat syndrome and other abnormalities of B chromosomes]. Nihon Rinsho (1978) 0.75
[Crying cat syndrome]. Paediatr Univ Tokyo (1965) 0.75
Screening for autosomal aberrations. Acta Paediatr Scand (1977) 0.75
Y-chromatin in aged males. Jinrui Idengaku Zasshi (1972) 0.75
[Heredity in Down's syndrome]. Saishin Igaku (1968) 0.75
Mental retardation, absence of patellae, and other malformations with chromosomal mosaicism. A follow-up report. J Pediatr (1968) 0.75
A de novo translocation t(6q+; 15q-) in a boy with trisomy 21. Jinrui Idengaku Zasshi (1975) 0.75
[Heteromorphism of human chromosomes and its clinical application II. The frequencies of chromosome variants (author's transl)]. Jinrui Idengaku Zasshi (1974) 0.75
A ring chromosome 9 in an infant with malformations. Hum Genet (1979) 0.75
On the new policy for reports on chromosomal anomalies. Hum Genet (1980) 0.75
Quinacrine banding without a fluorescence microscope. Lancet (1977) 0.75
A case of distal 4q trisomy due to familial (4;5)(q31;p15) translocation. Jinrui Idengaku Zasshi (1978) 0.75
Paternity testing: blood group systems and DNA analysis by variable number of tandem repeat markers. J Forensic Sci (1990) 0.75
A new approach in the evaluation of C-positive variants in man. Jinrui Idengaku Zasshi (1979) 0.75
Participation of D-group chromosomes in satelite associations. Humangenetik (1974) 0.75
On the DNA replication pattern of the Ph1 chromosome. Paediatr Univ Tokyo (1968) 0.75
[Cat cry syndrome]. Nihon Rinsho (1977) 0.75
[Banding studies in malformed patients with a "normal" karyotype (author's transl)]. Jinrui Idengaku Zasshi (1974) 0.75
21 trisomy and prenatally diagnosed XXY in two consecutive pregnancies. Hum Hered (1973) 0.75
Polyploidy in cultured amniotic-fluid cells. Lancet (1972) 0.75
[Dissociation from a fixed pattern in nursing]. Kango (1980) 0.75