(Q51963465)

English

Possible case of Pitt-Hopkins syndrome in sibs.

scientific article published in October 2001

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Possible case of Pitt-Hopkins syndrome in sibs. (English)

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Pitt-Hopkins syndrome

1 reference

based on heuristic

inferred from title

author name string

Orrico A

1

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Galli L

2

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Zappella M

3

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Lam CW

4

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Bonifacio S

5

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Torricelli F

6

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Hayek G

7

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

publication date

1 October 2001

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

103

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

2

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

157-159

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Mental retardation, "coarse" face, and hyperbreathing: confirmation of the Pitt-Hopkins syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Mental retardation, macrostomia and hyperpnoea syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Staining of human telomeres with primed in situ labeling (PRINS)

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1523

21 January 2018

Identifiers

10.1002/AJMG.1523

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/11568923

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