Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci. - Wikidata - wikimedia - TriplyDB

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

http://www.wikidata.org/entity/Q33595981

about

Neural crest and olfactory system: new prospective Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes Carrier detection in X linked ocular albinism using linked DNA polymorphisms.

P2860

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P2860

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

http://www.wikidata.org/entity/Q33595981

description

1993 nî lūn-bûn

@nan

1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1993 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

1993年の論文

@ja

1993年論文

@yue

1993年論文

@zh-hant

1993年論文

@zh-hk

1993年論文

@zh-mo

1993年論文

@zh-tw

1993年论文

@wuu

name

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@ast

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@en

type

label

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@ast

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@en

prefLabel

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@ast

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@en

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P1433

Journal of Medical Genetics

P1476

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

@en

P2093

A T Moore

http://www.w3.org/2001/XMLSchema#string

D E Barton

http://www.w3.org/2001/XMLSchema#string

J R Yates

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J S Green

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R McMahon

http://www.w3.org/2001/XMLSchema#string

S J Charles

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Y Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

Strategies for multilocus linkage analysis in humans

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Long-range restriction map of the terminal part of the short arm of the human X chromosome

Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene

Clinical features of affected males with X linked ocular albinism.

P304

923-925

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scholarly article

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10.1136/JMG.30.11.923

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11

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30

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1993-11-01T00:00:00Z

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14896945

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8301646

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P932

1016600

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