Pages that link to "Q34184149"
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The following pages link to The characterization of high-resolution G-banded chromosomes of man (Q34184149):
Displaying 50 items.
- cDNA cloning, expression and chromosomal localization of the human sarco/endoplasmic reticulum Ca(2+)-ATPase 3 gene (Q24324213) (← links)
- Human proto-oncogene c-mos maps to 8q11 (Q24555799) (← links)
- Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15 (Q28279431) (← links)
- Microcytogenetics 1984 (Q28300083) (← links)
- A possible exception to the critical region hypothesis. (Q30445592) (← links)
- Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes (Q33245366) (← links)
- Cell cycle synchronization: reversible induction of G2 synchrony in cultured rodent and human diploid fibroblasts (Q33256214) (← links)
- Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis. (Q33439914) (← links)
- High resolution of a small pericentric inversion of chromosome 11. (Q33667674) (← links)
- The fragile X: a scanning electron microscope study (Q33670739) (← links)
- Interstitial deletion and ring chromosome derived from 16q. (Q33674926) (← links)
- The 'morbid anatomy' of the human genome: tracing the observational and representational approaches of postwar genetics and biomedicine the William Bynum Prize Essay (Q33919847) (← links)
- Regional chromosomal assignment of human 3-beta-hydroxy-5-ene steroid dehydrogenase to 1p13.1 by non-isotopic in situ hybridisation (Q34128092) (← links)
- Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations (Q34273160) (← links)
- The Sonoda-Tajima Cell Collection: a human genetics research resource with emphasis on South American indigenous populations (Q34760052) (← links)
- Wilms's tumour and aniridia: clinical and cytogenetic features (Q35116296) (← links)
- Hypopigmentation in the Prader-Willi syndrome (Q35199084) (← links)
- Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center. (Q35199731) (← links)
- Distribution of break points in human structural rearrangements. (Q35202630) (← links)
- Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6. (Q35246214) (← links)
- Evidence of an epigenetic origin for high-risk 1q21 copy number aberrations in multiple myeloma (Q35724013) (← links)
- Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient (Q35889797) (← links)
- Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study (Q36258020) (← links)
- Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block (Q36640937) (← links)
- Early and late replication patterns of increased resolution in human lymphocyte chromosomes (Q36655808) (← links)
- Structure of human chromosomes visualized at the electron microscopic level (Q36657956) (← links)
- Sister chromatid differentiation in 5-bromo-2'-deoxyuridine-substituted chromosomes: a study with DNA-specific ligands and monoclonal antibody to histone H2B. (Q36677329) (← links)
- Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome (Q37540438) (← links)
- Gene mapping and leader polypeptide sequence of human glucocerebrosidase: implications for Gaucher disease. (Q37552855) (← links)
- Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH). (Q38501172) (← links)
- Dominant expansion of a cryptic subclone with an abnormal karyotype in B lymphoblastoid cell lines during culture (Q39249091) (← links)
- Relation between the SCE points and the DNA replication bands (Q39567101) (← links)
- Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literature (Q39758369) (← links)
- A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies (Q40126786) (← links)
- Chromosomal Location of Immunoglobulin Genes: Partial Mapping of These Genes in The Rabbit and Comparison With 1g Genes Carrying Chromosomes of Man and Mouse (Q40179126) (← links)
- Structural characteristics of genome organization in amphibians: differential staining of chromosomes and DNA structure (Q40334519) (← links)
- Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature (Q40442680) (← links)
- Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line (Q40724015) (← links)
- High-resolution fluorescence in situ hybridization: a new approach in genome mapping (Q41056654) (← links)
- Chromosomes and cancer: new nomenclature and future directions (Q41470098) (← links)
- Effect of colcemid exposure and methanol acetic acid fixation on human metaphase chromosome structure (Q41563435) (← links)
- Position of the human X inactivation center on Xq (Q41737215) (← links)
- Genes Coding for Histone Proteins in Man Are Located on the Distal End of the Long Arm of Chromosome 7 (Q41760312) (← links)
- De novo reciprocal translocation t(6;14)(q27;q13.3) in a child with infantile spasms (Q41933930) (← links)
- Aniridia, mental retardation and an unbalanced reciprocal translocation of chromosomes 8 and 11 with an interstitial deletion of 11p. (Q41935651) (← links)
- Karyotypic and fluorescent in situ hybridization study of the centromere of chromosome 7 in secondary myeloid neoplasms (Q42194645) (← links)
- Elongated mouse chromosomes suitable for enhanced molecular cytogenetics (Q42326861) (← links)
- Abnormalities of human chromosome 13 and in vitro radiosensitivity A study of 19 fibroblast strains (Q42802007) (← links)
- Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML. (Q43507348) (← links)
- Fluorescence in situ hybridisation analysis of sex chromosome in non-obstructive azoospermic men. (Q43965016) (← links)