(Q52075144)

21 April 2018

title

Further evidence for genetic heterogeneity in the fragile X syndrome. (English)

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21 April 2018

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W T Brown

1

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21 April 2018

E C Jenkins

2

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21 April 2018

A C Gross

3

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21 April 2018

C B Chan

4

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21 April 2018

M S Krawczun

5

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21 April 2018

C J Duncan

6

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21 April 2018

S L Sklower

7

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21 April 2018

G S Fisch

8

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21 April 2018

publication date

1 April 1987

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21 April 2018

published in

Human Genetics

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21 April 2018

volume

75

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21 April 2018

issue

4

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21 April 2018

page(s)

311-321

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21 April 2018

The prenatal detection of the fragile X chromosome: review of recent experience

cites work

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12 December 2020

Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX

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12 December 2020

High resolution banding and the locus of the Xq fragile site

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12 December 2020

X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data

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12 December 2020

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

1 reference

12 December 2020

The marker (X) syndrome: a cytogenetic and genetic analysis.

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12 December 2020

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

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12 December 2020

Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis

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12 December 2020

Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.

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12 December 2020

The genetic linkage map of the human X chromosome

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12 December 2020

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

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12 December 2020

Fragile X-linked mental retardation: the Martin-Bell syndrome

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12 December 2020

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications

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12 December 2020

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

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12 December 2020

The strength of association between fragile (X) chromosome presence and mental retardation

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12 December 2020

Feasibility of fragile X chromosome prenatal diagnosis demonstrated

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12 December 2020

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

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12 December 2020

The fragile (X) syndrome: the mutation problem

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12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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12 December 2020

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

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12 December 2020

Conference report: International Workshop on the fragile X and X-linked mental retardation.

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12 December 2020

Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation

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12 December 2020

Recombination between the fragile site Xq27 and the gene for coagulation factor IX

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12 December 2020

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

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12 December 2020

Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I

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12 December 2020

First trimester prenatal diagnosis of a male fetus with fragile X

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12 December 2020

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

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12 December 2020

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.

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12 December 2020

On the gates of hell and a most unusual gene

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12 December 2020

The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity

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12 December 2020

Genetic control over fragile X chromosome expression

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12 December 2020

Easy calculations of lod scores and genetic risks on small computers

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12 December 2020

Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male

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12 December 2020

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

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12 December 2020

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

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12 December 2020

Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage

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12 December 2020

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

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12 December 2020

Experience with prenatal fragile X detection

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12 December 2020

An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis

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12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

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12 December 2020

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

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12 December 2020

Learning disabilities and attentional problems in boys with the fragile X syndrome.

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12 December 2020

Identifiers

DOI

10.1007/BF00284100

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21 April 2018

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21 April 2018