(Q46324939)

21 December 2017

title

Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database (English)

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21 December 2017

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12

Joseph A Gogos

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21 December 2017

author name string

Maria Karayiorgou

1

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21 December 2017

Marie Torrington

2

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21 December 2017

Gonçalo R Abecasis

3

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21 December 2017

Herman Pretorius

4

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21 December 2017

Brian Robertson

5

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21 December 2017

Sean Kaliski

6

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21 December 2017

Stephen Lay

7

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21 December 2017

Christina Sobin

8

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21 December 2017

Natalie Möller

9

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21 December 2017

S Laura Lundy

10

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21 December 2017

Maude L Blundell

11

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21 December 2017

J Louw Roos

13

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21 December 2017

publication date

1 January 2004

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21 December 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

published in

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21 December 2017

volume

124B

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21 December 2017

page(s)

20-28

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21 December 2017

issue

1

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21 December 2017

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Linkage disequilibrium analysis in a recently founded population: evaluation of the variegate porphyria founder in South African Afrikaners

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Extended intermarker linkage disequilibrium in the Afrikaners

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint maps to an 11-cM region on chromosome 4q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Early, non-psychotic deviant behavior in schizophrenia: a possible endophenotypic marker for genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.20090

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.20090

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21 December 2017

PubMed ID

14681908

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21 December 2017