Further segregation analysis of the fragile X syndrome with special reference to transmitting males (Q34192224)

31 July 2017

title

Further segregation analysis of the fragile X syndrome with special reference to transmitting males. (English)

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31 July 2017

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3

Morton NE

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31 July 2017

Sherman SL

1

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31 July 2017

Jacobs PA

2

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31 July 2017

Froster-Iskenius U

4

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31 July 2017

Howard-Peebles PN

5

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31 July 2017

Nielsen KB

6

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31 July 2017

Partington MW

7

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31 July 2017

Sutherland GR

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31 July 2017

Turner G

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31 July 2017

Watson M

10

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31 July 2017

publication date

1 January 1985

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31 July 2017

language of work or name

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31 July 2017

volume

69

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31 July 2017

issue

4

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31 July 2017

page(s)

289-299

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

31 July 2017

cites work

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Additional evidence for fragile X activity in heterozygous carriers.

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Familial X-linked mental retardation with an X chromosome abnormality

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

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Hereditary retinoblastoma: delayed mutation or host resistance?

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Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

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Transition matrices with mutation

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

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

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Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

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Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation

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

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Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

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Marker X-associated mental retardation. A study of 150 retarded males.

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Fragile X in a normal male: a cautionary tale

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

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Feasibility of fragile X chromosome prenatal diagnosis demonstrated

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Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females

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X-linked mental retardation associated with macro-orchidism

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Familial X-linked mental retardation and fragile X chromosomes in two Swedish families

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Escalante syndrome and the marker X chromosome

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Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation

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Complex Segregation Analysis with Pointers

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Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy

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The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation

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

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Mutation and selection in the marker (X) syndrome. A hypothesis

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Familial X-linked mental retardation, verbal disability, and marker X chromosomes

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A possible case of delayed mutation in man

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Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.

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Activity of the fragile X in heterozygous carriers

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A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

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Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families

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

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The fragile X chromosome in a large Indian kindred.

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X-linked mental retardation: a study of 7 families

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Genetic epidemiology of Lesch-Nyhan disease

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Fragile X trait in a large kindred: transmission also through normal males

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12 December 2020

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

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A marker X chromosome

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

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12 December 2020

X-linked mental retardation with macro-orchidism and marker X chromosomes

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12 December 2020

Replication pattern in XXY cells with fra(X)

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12 December 2020

Identifiers

DOI

10.1007/BF00291644

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Dimensions Publication ID

31 July 2017

1004855369

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