(Q28278781)

1

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Z Kraiem

2

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J C Beck

3

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D Nishimura

4

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E M Stone

5

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M Salameh

6

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O Sadeh

https://scigraph.springernature.com/pub.10.1038/ng0496-424

7

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language of work or name

English

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publication date

April 1996

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published in

Nature Genetics

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volume

12

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page(s)

424-6

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issue

4

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exact match

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cites work

Association of congenital deafness with goitre; the nature of the thyroid defect.

1 reference

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Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

21 January 2018

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Novel approaches to linkage mapping.

21 January 2018

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Monoamine oxidase activity and triiodothyronine biosynthesis in human cultured thyroid cells

21 January 2018

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Deafness with sporadic goiter. Pendred's syndrome.

21 January 2018

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7 January 2021

Fifteen cases of Pendred's syndrome. Congenital deafness and sporadic goiter.

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7 January 2021

Clinical and molecular genetics studies in Pendred's syndrome.

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7 January 2021

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

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7 January 2021

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

1 reference

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7 January 2021

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter

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7 January 2021

Genetic Linkage Studies of Thyroid Peroxidase (TPO) Gene in Families with TPO Deficiency*

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7 January 2021

Normal peroxidase activity in Pendred's syndrome

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Biochemical studies on the iodine organification defect of Pendred's syndrome

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7 January 2021

A patient with dup(10p)del(8q) and Pendred syndrome

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7 January 2021

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism

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7 January 2021

Studies on the Thyroidal Defect in an Atypical Form of Pendred's Syndrome*

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7 January 2021

Iodide uptake and organification, tri-iodothyronine secretion, cyclic AMP accumulation and cell proliferation in an optimized system of human thyroid follicles cultured in collagen gel suspended in serum-free medium

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7 January 2021

Mutual antagonistic interactions between the thyrotropin (adenosine 3',5'-monophosphate) and protein kinase C/epidermal growth factor (tyrosine kinase) pathways in cell proliferation and differentiation of cultured human thyroid follicles

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7 January 2021

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

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7 January 2021

Fast and sensitive silver staining of DNA in polyacrylamide gels

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7 January 2021

Programs for pedigree analysis: Mendel, Fisher, and dGene

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7 January 2021

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

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7 January 2021