(Q50343305)

English

Brief report: screening children with autism for fragile-X syndrome and phenylketonuria

scientific article published in September 1985

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

Brief report: screening children with autism for fragile-X syndrome and phenylketonuria (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

0 references

phenylketonuria

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

S M Pueschel

1

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

R Herman

2

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

G Groden

3

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

language of work or name

0 references

publication date

1 September 1985

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

15

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

3

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

335-338

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

Sex ratios in families of autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X chromosome and autistic mental retardation. Apropos of 23 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Causes of infantile autism: some considerations from recent research

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of phenylketonuria in autistic and psychotic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood psychosis and neurofibromatosis--more than a coincidence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism is associated with the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurological findings in patients with the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical triplets with infantile autism and the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile autism associated with the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4030666

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01531503

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/4030666

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50343305&oldid=2248295876"