(Q52096702)

English

Screening for fra(X)(q) in a population of mentally retarded males.

scientific article published in January 1983

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

Screening for fra(X)(q) in a population of mentally retarded males. (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

author name string

U Froster-Iskenius

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

G Felsch

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

C Schirren

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

E Schwinger

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

publication date

1 January 1983

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

63

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

153-157

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication pattern in XXY cells with fra(X)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial sex-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An anatomic approach to the obtrusive ear

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

More on marker X chromosomes, mental retardation and macro-orchidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fragile X syndrome by testicular size measurement

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonspecific X-linked mental retardation II: the frequency in British Columbia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The growth pattern of the external ear

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of fragile (X) (q27) site from a male

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: Transmission of the trait by an apparently unaffected male

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X in a normal male: a cautionary tale

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker X syndrome in an oriental family with probable transmission by a normal male.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6682403

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291535

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6682403

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