(Q68353287)

English

Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study

scientific article published on 01 August 1990

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scholarly article

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23 September 2019

Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study (English)

1 reference

Europe PubMed Central

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23 September 2019

author name string

H J Decker

1

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23 September 2019

L A Cannizzaro

2

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23 September 2019

M J Mendez

3

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23 September 2019

S P Leong

4

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23 September 2019

H Bixenman

5

1 reference

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23 September 2019

C Berger

6

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23 September 2019

A A Sandberg

7

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23 September 2019

publication date

1 August 1990

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23 September 2019

1 reference

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23 September 2019

85

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23 September 2019

337-342

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23 September 2019

3

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23 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00206758

0 references

Cell culture studies on neurofibromatosis (von Recklinghausen). V. Monosomy 22 and other chromosomal anomalies in cultures from peripheral neurofibromas

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumors of the peripheral nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the G-CSF gene on chromosome 17 proximal to the breakpoint in the t(15;17) in acute promyelocytic leukemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous level of sister chromatid exchanges in patients with tuberous sclerosis and Recklinghausen's neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of chromosomal instability in neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis: clinical heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Von Recklinghausen neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis: no chromosomal defect by prophase banding technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precise localization of NF1 to 17q11.2 by balanced translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis and chromosomal translocation. Report of a case of 46, XX,t(2p-:22p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sister chromatid exchanges and chromosome aberrations in von Recklinghausen's disease--a family study

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rearranged transforming gene, tre, is made up of human sequences derived from chromosome regions 5q, 17q and 18q

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of NF1 to 12 chromosome 17 markers: a summary of eight concurrent reports

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human G-CSF gene to 17q11 proximal to the breakpoint of the t(15;17) in acute promyelocytic leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic clones in a recurrent neurofibroma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignancy in neurofibromatosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The chromosomal findings in seven human neurinomas and one neurosarcoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A female patient with translocation 46, XX, t(Dq-; Bq+) and neurofibromatosis, imbecility and aortic coarctation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human gene coding for granulocyte-colony stimulating factor is assigned to the q21-q22 region of chromosome 17.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved method for G-banding chromosomes after in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human homeo box-containing genes located at chromosome regions 2q31----2q37 and 12q12----12q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple cytogenetic aberrations in neurofibrosarcomas complicating neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome changes in soft tissue sarcomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis in a man with a ring 22: in situ hybridization studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2118474

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00206758

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2118474%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2118474%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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