Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17

Genomics

Volumn 5, Issue 2, 1989, Pages 245-249

  Menon, Anil G ^a,b   Ledbetter, David H ^c   Rich, Donna C ^c   Seizinger, Bernd R ^a,b   Rouleau, Guy A ^a,b   Michels, Virginia F ^d   Schmidt, Michael A ^d   Dewald, Gordon ^d   DallaTorre, Camille M ^a,b   Haines, Jonathan L ^a,b   Gusella, James F ^a,b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ARTICLE; CHROMOSOME 17; CHROMOSOME TRANSLOCATION; FEMALE; GENETIC MARKER; GENETICS; HUMAN; HYBRID CELL; MOUSE; NEUROFIBROMATOSIS; RESTRICTION MAPPING;

ANIMAL; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENETIC MARKERS; HUMAN; HYBRID CELLS; MICE; NEUROFIBROMATOSIS 1; RESTRICTION MAPPING; SUPPORT, U.S. GOV'T, P.H.S.; TRANSLOCATION (GENETICS);

EID: 0024712191     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(89)90053-0     Document Type: Article

References (20)

1. Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids
2. Gene for von Reckling-hausen neurofibromatosis is in the pericentric region of chromosome 17
3. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy
4. A genetic linkage map for 27 loci from PND to FY on the short arm of chromosome 1
5. The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints
6. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
7. Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17
8. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
9. Multipoint linkage analysis in neurofibromatosis type 1: An international collaboration
10. Precise localization of NF1 to 17q11.2 by balanced translocation
11. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
12. Von Recklinghausen neurofibromatosis
13. Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location
14. Cases of neurofibromatosis with rearrangements of chromosome 17 involving band 17q11.2
15. Removal of repeated sequences from hybridisation probes
16. Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene
17. Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)
18. Regional mapping panel for human chromosome 17: Application of neurofibromatosis type 1