| scholarly article | Q13442814 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/bf00273835 |
| P698 | PubMed publication ID | 3026946 |
| P2093 | author name string | J Schmidtke | |
| M Krawczak | |||
| F Hanefeld | |||
| E Seemanova | |||
| E Wilichowski | |||
| P2860 | cites work | Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy | Q59080076 |
| Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy | Q69841265 | ||
| Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9) | Q70096800 | ||
| Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy | Q70096806 | ||
| Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families | Q70101098 | ||
| Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy | Q70180244 | ||
| Localisation of gene for Becker muscular dystrophy | Q72567340 | ||
| [A new x-chromosomal muscular dystrophy] | Q73787710 | ||
| Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase | Q24301432 | ||
| Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
| Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I | Q27860885 | ||
| Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm | Q33584511 | ||
| Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus | Q33669145 | ||
| Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome | Q33671990 | ||
| Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids | Q35199786 | ||
| A strategy to reveal high-frequency RFLPs along the human X chromosome | Q35199942 | ||
| Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome | Q35200261 | ||
| Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21. | Q35201570 | ||
| Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies | Q35570490 | ||
| Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome | Q35674421 | ||
| Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy | Q36132993 | ||
| Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci | Q36423476 | ||
| Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy | Q36423501 | ||
| Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment | Q36423793 | ||
| Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention | Q40170529 | ||
| An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695. | Q42802382 | ||
| Report of the Committee on the Genetic Constitution of the X and Y Chromosomes | Q44429358 | ||
| Restriction fragment length polymorphisms at the human parathyroid hormone gene locus | Q57264028 | ||
| P433 | issue | 1 | |
| P921 | main subject | Becker muscular dystrophy | Q2484592 |
| P304 | page(s) | 32-40 | |
| P577 | publication date | 1987-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers | |
| P478 | volume | 75 |
| Q69922941 | Linkage relationship between retinoschisis and four marker loci |
| Q35198256 | Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes |
| Q34164340 | Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome. |
| Q60641490 | Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β |
| Q33677883 | X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred |
Search more.