| scholarly article | Q13442814 |
| P953 | full work available at URL | https://europepmc.org/articles/PMC1702407 |
| https://europepmc.org/articles/PMC1702407?pdf=render | ||
| https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1746553/?tool=EBI | ||
| https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1746553/pdf/?tool=EBI | ||
| P932 | PMC publication ID | 1702407 |
| P698 | PubMed publication ID | 1746553 |
| P50 | author | James F. Gusella | Q1602688 |
| P2093 | author name string | F. F. Elder | |
| F. Greenberg | |||
| D. H. Ledbetter | |||
| J. J. Wasmuth | |||
| U. Bengtsson | |||
| M. R. Altherr | |||
| M. E. McDonald | |||
| P2860 | cites work | "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 |
| Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4. | Q33675382 | ||
| Microdeletion syndromes, balanced translocations, and gene mapping | Q33676997 | ||
| Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation | Q33837049 | ||
| Deficiency on the short arms of a chromosome No. 4 | Q34241073 | ||
| Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion | Q34241369 | ||
| Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization | Q35196840 | ||
| Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5 | Q35197231 | ||
| Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus | Q35246016 | ||
| Clustering of multiallele DNA markers near the Huntington's disease gene | Q35814879 | ||
| Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries | Q36438141 | ||
| The Wolf-Hirschhorn syndrome. I. Genetics. | Q40362613 | ||
| Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. | Q42507687 | ||
| Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene | Q45296147 | ||
| A highly polymorphic locus very tightly linked to the Huntington's disease gene | Q45296953 | ||
| Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines | Q45795446 | ||
| Simultaneous identification and banding of human chromosome material in somatic cell hybrids. | Q46016519 | ||
| Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease | Q46988213 | ||
| Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)] | Q72032778 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Wolf-Hirschhorn syndrome | Q610075 |
| human chromosome 4 | Q836605 | ||
| chromosomal translocation | Q916504 | ||
| P304 | page(s) | 1235-1242 | |
| P577 | publication date | 1991-12-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4 | |
| P478 | volume | 49 |
| Q35196100 | A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype |
| Q33675551 | A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat |
| Q33594186 | A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation. |
| Q34605651 | Chromosome break-induced DNA replication leads to nonreciprocal translocations and telomere capture. |
| Q40541891 | Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms |
| Q33921096 | Dopamine receptor genes: new tools for molecular psychiatry. |
| Q33683305 | Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study |
| Q33682657 | Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features |
| Q38635880 | Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations. |
| Q35195763 | Minireview: cryptic translocations and telomere integrity |
| Q33673183 | Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome |
| Q35540299 | Molecular cytogenetic analysis of telomere rearrangements |
| Q35195824 | Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome |
| Q33941622 | Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis |
| Q35140834 | Phenotypic variations in wolf-hirschhorn syndrome |
| Q33679121 | Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3. |
| Q24798749 | Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity |
| Q41536160 | Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability. |
| Q33595849 | Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis |
| Q42769365 | Screening chromosome ends for learning disability |
| Q35432422 | Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres |
| Q45289080 | Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5. |
| Q40673742 | Toward the complete genomic map and molecular pathology of human chromosome 4. |
Search more.