(Q36721514)

English

Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome

scientific article published on March 1994

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

5

object named as

J P Dumanski

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

author name string

H Kurahashi

1

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

K Akagi

2

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

K Karakawa

3

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

T Nakamura

4

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

T Sano

6

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

S Okada

7

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

S Takai

8

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

I Nishisho

9

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

publication date

1 March 1994

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

93

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

248-254

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic changes and histopathological types in colorectal tumors from patients with familial adenomatous polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a long-range map of human chromosomal band 22q11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of the long arm of human chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the Philadelphia chromosome by gene mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and mapping of 62 new RFLP markers on human chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the supernumerary chromosome in cat eye syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased tumorigenicity of rodent cells after fusion with leukocytes from normal and leukemic donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/7907312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00212017

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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