Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis. - Wikidata - awgldk - TriplyDB

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

http://www.wikidata.org/entity/Q33683279

about

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism.Hypomelanosis of Ito: clinical syndrome or just phenotype?An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito.Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.Genetic control of X inactivation and processes leading to X-inactivation skewing.Incontinentia pigmenti versus hypomelanosis of Ito: the whys and wherefores of a confusing issue.Pigmentary mosaicism of the hyperpigmented type in two half-brothers.Linear and whorled nevoid hypermelanosis with bilateral giant cerebral aneurysms

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P2860

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

http://www.wikidata.org/entity/Q33683279

description

1996 nî lūn-bûn

@nan

1996 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի մարտին հրատարակված գիտական հոդված

@hy

1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年论文

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name

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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type

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Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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prefLabel

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

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Hatchwell E

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P2860

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase

A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

Three patients with ring (X) chromosomes and a severe phenotype.

Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings.

Inherited partial X chromosome duplication in a mentally retarded male

A de novo X;13 translocation with abnormal phenotype

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp.

Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.

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