(Q52090619)

English

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site. (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

author name string

M G Mattei

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

M A Baeteman

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

R Heilig

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

I Oberlé

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

K Davies

5

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

J L Mandel

6

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

J F Mattei

7

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

number of pages

5

1 reference

based on heuristic

inferred from page(s)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

69

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

327-331

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

describes a project that uses

in situ hybridization

1 reference

based on heuristic

inferred from title

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a unique gene by direct hybridization in situ

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation with the fragile X. A study of 15 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of DNA replication of human chromosomes. II. Replication map and replication model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the thyroglobulin gene by in situ hybridization to human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the human factor IX gene by molecular hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://pubmed.ncbi.nlm.nih.gov/2985491

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291650

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2985491

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