(Q50344098)

English

Gene mapping studies with the syndrome of autism.

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

Gene mapping studies with the syndrome of autism. (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

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author name string

M A Spence

1

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

E R Ritvo

2

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

M L Marazita

3

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

S J Funderburk

4

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

R S Sparkes

5

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

B J Freeman

6

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

language of work or name

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publication date

1 January 1985

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Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

Behavior Genetics

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Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

15

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

1

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

1-13

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

The 1983 catalogue of mapped human genetic markers and report of the Nomenclature Committee.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and immunohematologic factors in autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

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/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics, if any, of infantile autism and childhood schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New C band markers of human chromosomes: C band position variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A computer program for linkage analysis of general human pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Current research on the syndrome of autism: introduction. The National Society for Autistic Children's definition of the syndrome of autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic influences and infantile autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple technique for demonstrating centromeric heterochromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual

1 reference

https://pubmed.ncbi.nlm.nih.gov/3985910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01071928

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 March 2018

http://europepmc.org/abstract/MED/3985910

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