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Heterozygote
Known as:
heterozygous genotype
, Heterozygous
, Heterozygosity
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Occurs when the two alleles at a particular gene locus are different. A heterozygous genotype may include one normal allele and one mutation, or two…
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National Institutes of Health
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Related topics
Related topics
4 relations
Broader (1)
Genotype
Heterozygote Detection
Hybrid Vigor
Hybrids
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
Characterization of Spanish grapevine cultivar diversity using sequence-tagged microsatellite site markers.
J. Martín
,
J. Borrego
,
F. Cabello
,
J. M. Ortiz
Genome
2003
Corpus ID: 23278444
A broad germplasm bank collection containing most of the autochthonous Spanish grapevine cultivars was analyzed using six…
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Review
1997
Review
1997
Screening for CDKN2A mutations in hereditary melanoma.
A. Goldstein
,
M. Tucker
Journal of the National Cancer Institute
1997
Corpus ID: 45718753
Cutaneous malignant melanoma (CMM) is a potentially fatal form of skin cancer whose etiology is heterogeneous and complex…
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Highly Cited
1995
Highly Cited
1995
Identification of multiple breast cancers of multicentric origin by histological observations and distribution of allele loss on chromosome 16q.
H. Tsuda
,
S. Hirohashi
Cancer Research
1995
Corpus ID: 46564351
Breast cancer is often detected as multiple lesions clinically and/or histopathologically. To examine if the origin of such…
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Highly Cited
1993
Highly Cited
1993
Genetic variation within and between two Tyrrhenian populations of the Mediterranean alcyonarian Corallium rubrum
M. Abbiati
,
G. Santangelo
,
S. Novelli
1993
Corpus ID: 24888854
Allozymic variation of 13 gene loci was investigated in 2 samples of Corallium rubrum (L.) collected in the Tyrrhenian Sea…
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Highly Cited
1986
Highly Cited
1986
Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13.
J. Squire
,
T. Dryja
,
+7 authors
R. A. Phillips
Proceedings of the National Academy of Sciences…
1986
Corpus ID: 23226518
The study of recessive oncogenes such as those responsible for retinoblastoma and Wilms tumor is difficult because the gene…
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Highly Cited
1985
Highly Cited
1985
Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?
Z. Laron
,
M. Kelijman
,
A. Pertzelan
,
R. Keret
,
J. Shoffner
,
J. Parks
Israel journal of medical sciences
1985
Corpus ID: 23593056
Using restriction endonuclease analysis of genomic DNA hybridized to a human chorionic somatomammotropin (hCS) complementary (c…
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Highly Cited
1985
Highly Cited
1985
Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution.
M. Koenig
,
J. Moisan
,
R. Heilig
,
J. Mandel
Nucleic Acids Research
1985
Corpus ID: 2285316
We have isolated and characterized DNA probes that detect homologies between the X and Y chromosomes. Clone St25 is derived from…
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Review
1978
Review
1978
Population genetic studies of the Philippine Negritos. I. A pilot survey of red cell enzyme and serum protein groups.
K. Omoto
,
S. Misawa
,
S. Harada
,
J. Sumpaico
,
P. Medado
,
H. Ogonuki
American Journal of Human Genetics
1978
Corpus ID: 22120815
Electrophoretic surveys of red cell enzyme and serum protein systems representing 21 genetic loci were carried out on 129 blood…
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Highly Cited
1973
Highly Cited
1973
Biochemical polymorphism and systematics in the genus Peromyscus. 3. Variation in the Florida deer mouse (Peromyscus floridanus), a pleistocene relict.
M. H. Smith
,
R. Selander
,
W. Johnson
Journal of Mammalogy
1973
Corpus ID: 35004115
Electrophoretically demonstrable variation was analyzed in proteins encoded by 41 structural gene loci in 71 individuals of the…
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Highly Cited
1970
Highly Cited
1970
Meiotic nondisjunction in mice and mouse hybrids.
U. Tettenborn
,
A. Gropp
Cytogenetics
1970
Corpus ID: 33988282
Nondisjunction in the first meiotic division was evaluated by the frequency of aneuploid metaphase II (M II) figures in secondary…
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