Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation (Q50313187)

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scientific article published in February 2000

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Language	Label	Description	Also known as
English	Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation	scientific article published in February 2000

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

title

Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

main subject

autism

0 references

bipolar disorder

1 reference

based on heuristic

inferred from title

Tourette syndrome

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based on heuristic

inferred from title

author name string

Kerbeshian J

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

Severud R

series ordinal

2

1 reference

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Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

Burd L

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

Larson L

series ordinal

4

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Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

publication date

1 February 2000

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Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

published in

American Journal of Medical Genetics Part A

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stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

volume

96

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

page(s)

69-73

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Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

cites work

A prevalence study of pervasive developmental disorders in North Dakota

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Childhood Onset Pervasive Developmental Disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Children with Fetal Alcohol Syndrome in North Dakota: a case control study utilizing birth certificate data

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

A prevalence study of Rett syndrome in an institutionalized population

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Comparisons of DSM-III defined pervasive developmental disorders in North Dakota children.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: the key to understand the genetics of comorbid phenotypes?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Increased chromosomal breakage in Tourette syndrome predicts the possibility of variable multiple gene involvement in spectrum phenotypes: preliminary findings and hypothesis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Differential responsiveness to lithium in patients with Tourette disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Comorbid Tourette's disorder and bipolar disorder: an etiologic perspective.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Huntington disease and childhood-onset Tourette syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

The fragile site on chromosome 16 (q21q22). Data on four new families

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Different inducibility and possible significance of several concomitant "fragile sites" in two brothers

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Fragile site long arm chromosome 16

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Gilles de la Tourette's syndrome and bipolar disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Prevalence of Gilles de la Tourette's syndrome in North Dakota adults

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

A new location for the human adenine phosphoribosyltransferase gene ( APRT ) distal to the haptoglobin ( HP ) and fra(16)(q23) ( FRAUD ) loci

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Bilineal transmission and phenotypic variation of Tourette's disorder in a large pedigree

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

FISH mapping of a human chromosome 16 constitutional pericentric inversion inv(16)(p13q22) found in a large kindred

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000207%2996%3A1%3C69%3A%3AAID-AJMG14%3E3.0.CO%3B2-5

retrieved

21 January 2018

Identifiers

DOI

10.1002/(SICI)1096-8628(20000207)96:1<69::AID-AJMG14>3.0.CO;2-5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

PubMed publication ID

10686555

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10686555

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/10686555

 

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