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X-linked inheritance
Known as:
X-LINKED
, Inheritance, X Linked
, X Linked Inheritance
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A mode of inheritance that is observed for traits related to a gene encoded on the X chromosome. [HPO:curators]
National Institutes of Health
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Related topics
Related topics
27 relations
Akesson syndrome
Blood group deletion syndrome
Clark-Baraitser syndrome
Congenital atresia of colon
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Broader (1)
mendelian inheritance
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Modulation of gap junction channels and hemichannels by growth factors.
K. Schalper
,
M. Riquelme
,
+5 authors
J. Sáez
Molecular Biosystems
2012
Corpus ID: 24206255
Gap junction hemichannels and cell-cell channels have roles in coordinating numerous cellular processes, due to their…
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Review
1997
Review
1997
Advances in hereditary spastic paraplegia.
John K. Fink
Current Opinion in Neurology
1997
Corpus ID: 35598218
Hereditary spastic paraplegia refers to a group of clinically similar disorders whose primary feature is insidiously progressive…
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1996
1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.
L. White
,
Peter K. Rogan
,
R. D. Nicholls
,
Bai-lin Wu
,
Bruce R. Korf
,
J. H. Knoll
American Journal of Human Genetics
1996
Corpus ID: 37568298
Allele-specific replication differences have been observed in imprinted chromosomal regions. We have exploited this…
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Highly Cited
1992
Highly Cited
1992
Visual impairment in Nordic children
R. Riise
,
T. Flage
,
+4 authors
M. Warburg
Acta ophthalmologica
1992
Corpus ID: 34838142
Abstract. A Nordic study group of ophthalmologists, NORDSYN, has compiled data from registers in Denmark, Finland, Iceland and…
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Highly Cited
1983
Highly Cited
1983
Serum osteocalcin in the treatment of inherited rickets with 1,25-dihydroxyvitamin D3.
C. Gundberg
,
D. Cole
,
J. Lian
,
T. Reade
,
P. Gallop
Journal of Clinical Endocrinology and Metabolism
1983
Corpus ID: 2155178
Osteocalcin is a vitamin K-dependent protein, synthesized in bone, which can be detected in serum. We have measured circulating…
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1980
1980
A Source Book for Linkage in Man
M. Seashore
The Yale Journal of Biology and Medicine
1980
Corpus ID: 30507717
reveals the simplicity of that casual equation by detailing for us over a hundred inherited medical disorders known to afflict…
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Highly Cited
1978
Highly Cited
1978
Natural killing in immunodeficient patients.
H. Koren
,
D. Amos
,
R. Buckley
Journal of Immunology
1978
Corpus ID: 31946492
Natural killing (NK) capacity was evaluated in peripheral blood mononuclear cells from 14 patients with well defined primary…
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Highly Cited
1978
Highly Cited
1978
Demonstration of adenosine receptor on human lymphocytes in vitro and its possible role in the adenosine deaminase-deficient form of severe combined immunodeficiency.
A. Schwartz
,
R. Stern
,
S. Polmar
Clinical Immunology and Immunopathology
1978
Corpus ID: 27434012
Highly Cited
1970
Highly Cited
1970
Experimental myopathy after microarterial embolization; comparison with childhood x-linked pseudohypertrophic muscular dystrophy.
P. Hathaway
,
W. Engel
,
H. Zellweger
Archives of Neurology
1970
Corpus ID: 40193361
THE ETIOLOGY and pathogenesis of childhood x-linked pseudohypertrophic muscular dystrophy ("Duchenne dystrophy") remains obscure…
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1966
1966
X-Linked Recessive Inheritance of a Syndrome of Mental Retardation With Hyperuricemia
Samuel L. Shapiro
,
G. Sheppard
,
F. Dreifuss
,
D. Newcombe
Proceedings of the Society for Experimental…
1966
Corpus ID: 27195669
Summary A pedigree of a heritable metabolic disorder of uric acid overproduction indicated an x-linked recessive mode of…
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