Pages that link to "Q70000173"
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The following pages link to [Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine] (Q70000173):
Displaying 50 items.
- Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy (Q33186583) (← links)
- X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci (Q33584573) (← links)
- Trisomy 20p from maternal t(3;20) translocation (Q33584740) (← links)
- Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation (Q33586732) (← links)
- Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings (Q33587934) (← links)
- X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies (Q33588425) (← links)
- 47,XXX chromosome constitution in a male (Q33667714) (← links)
- Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings (Q33668144) (← links)
- X long arm deletion with oligomenorrhoea. (Q33669729) (← links)
- Cytological subdivision of the S phase of human cells in asynchronous culture (Q33671367) (← links)
- Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11. (Q33763900) (← links)
- Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis (Q34038290) (← links)
- Chromosomal evolution in Primates: Tentative phylogeny from Microcebus murinus (Prosimian) to man (Q34154155) (← links)
- Pericentric inversions. Problems and significance for clinical genetics (Q34709047) (← links)
- Photosensitizing dyes and fluorochromes as substitutes for 33258 Hoechst in the fluorescence-plus-Giemsa (FPG) chromosome technique (Q35017922) (← links)
- A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies (Q35199229) (← links)
- Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome (Q35200261) (← links)
- Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases (Q35202068) (← links)
- Patterns of DNA replication of human chromosomes. II. Replication map and replication model. (Q35202435) (← links)
- Normal and abnormal karyotypes of cattle (Q35219650) (← links)
- DNA denaturation for ultrastructural banding and the mechanism underlying the fluorochrome-photolysis-Giemsa technique studied with anti-5-bromodeoxyuridine antibodies (Q35591507) (← links)
- Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations (Q35830053) (← links)
- Replication timing, chromosomal bands, and isochores (Q36491164) (← links)
- Specific fluorescent bands on chromosomes produced by acridine orange after prestaining with base specific non-fluorescent DNA ligands (Q36589171) (← links)
- Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block (Q36640937) (← links)
- Quinacrine and acridine-R banding without a fluorescence microscope (Q36675014) (← links)
- BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes (Q36896171) (← links)
- Four new cases of X-autosome translocation in man (author's transl) (Q39337172) (← links)
- Analysis of the karyotype of Pan paniscus. Comparison with other Pongidae and man (author's transl) (Q39337262) (← links)
- Discontinued treatment with BudR and staining with acridine orange: observation of R- or Q- or intermediary banding (author's transl) (Q39349536) (← links)
- Various banding simultaneously obtained on the same slides, after treatment by BrdU (author's transl) (Q39371447) (← links)
- Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X). (Q39399924) (← links)
- Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment (Q39411395) (← links)
- Segmentation of human chromosomes induced by 5-ACR (5-azacytidine) (Q39411806) (← links)
- The relationship between DNA replication and chromosome structure (Q39427293) (← links)
- LBA technique in the detection of chromosome variants. I. Chromosomes with known sites of Q variants (Q39461681) (← links)
- Silver-staining specificity in metaphases after incorporation of 5-bromodeoxyuridine (BUDR). (Q39475207) (← links)
- Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21) (Q39893526) (← links)
- t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring (Q41038591) (← links)
- A case of trisomy 3q21?qter syndrome (Q41448890) (← links)
- Syndrome +12p. Case report and review (Q41551957) (← links)
- Hormonal studies in a male with a 47,XXX chromosome constitution: comparison with the hormonal pattern of a 46,XX male and patients with Klinefelter's syndrome (Q41599479) (← links)
- Partial trisomy 4q: Two cases with a familial translocation t(4;18)(q27;q23) (Q41684075) (← links)
- A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea (Q41684154) (← links)
- Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis (Q41737193) (← links)
- Duplication 15q22�15qter and its phenotypic expression (Q41935691) (← links)
- Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7 (Q41936555) (← links)
- Comparative mapping of ZFY in the hominoid apes (Q41986566) (← links)
- Two new estrogen-supersensitive variants of the MCF-7 human breast cancer cell line (Q42823206) (← links)
- BrdU-sensitive fragile site on long arm of chromosome 16. (Q43143432) (← links)