(Q34353426)

1 August 2017

1 reference

title

Strategies for the molecular genetic analysis of obesity in humans (English)

1 reference

1 August 2017

0 references

Leibel RL

1

1 reference

1 August 2017

Bahary N

series ordinal

2

1 reference

1 August 2017

Friedman JM

series ordinal

3

1 reference

1 August 2017

publication date

1 January 1993

1 reference

Critical Reviews in Food Science and Nutrition

1 August 2017

published in

1 reference

1 August 2017

volume

33

1 reference

1 August 2017

issue

4-5

1 reference

1 August 2017

page(s)

351-358

1 reference

Body-build and its inheritance

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Commingling analysis of obesity in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

An Adoption Study of Human Obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Genetics of obesity in adult adoptees and their biological siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Genetic contributions to human fatness: an adoption study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Prader-Willi syndrome: current understanding of cause and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Confirmation of the Cohen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

21 January 2018

New light on obesity.

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Set points for body weight and fat

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Tackling a weighty problem

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Construction of a general human chromosome jumping library, with application to cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Variable number of tandem repeat (VNTR) markers for human gene mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Microdissection and microcloning of mid-chromosome 4: genetic mapping of 41 microdissection clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Molecular mapping of the mouse db mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Molecular mapping of the mouse ob mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Rat obesity gene fatty (fa) maps to chromosome 5: evidence for homology with the mouse gene diabetes (db).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

The influence of genetic background on the expression of mutations at the diabetes locus in the mouse. III. Effect of H-2 haplotype and sex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Genetic analysis of glucose tolerance in inbred mouse strains. Evidence for polygenic control.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

The influence of genetic background on the expression of mutations at the diabetes locus in the mouse. V. Interaction between the db gene and hepatic sex steroid sulfotransferases correlates with gender-dependent susceptibility to hyperglycemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Type 1 diabetes in mice is linked to the interleukin-1 receptor and Lsh/lty/Bcg genes on chromosome 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

The Body-Mass Index of Twins Who Have Been Reared Apart

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408399309527632

10.1080/10408399309527632

21 January 2018

Identifiers

DOI

1 reference

1 August 2017

1 reference