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Wrinkly skin syndrome
Known as:
WSS
National Institutes of Health
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Related topics
Related topics
22 relations
Autosomal recessive inheritance
Byzanthine arch palate
Congenital clubfoot
Congenital pectus excavatum
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Broader (1)
Cutis Laxa
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A novel de novo mutation (p.Pro1310Glnfs*46) in KMT2A caused Wiedemann–Steiner Syndrome in a Chinese boy with postnatal growth retardation: a case report
Minghui Chen
,
Ruihong Liu
,
Chao Wu
,
Xunhua Li
,
Yiming Wang
Molecular Biology Reports
2019
Corpus ID: 195698954
Wiedemann–Steiner Syndrome (WSS) is a very rare autosomal dominant disease. Mutations in the KMT2A gene have been shown to cause…
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2009
2009
Synthesis of Zn2SiO4:Mn2+ green emission phosphor by hydrothermal gelation method using a novel water soluble silicon compound
N. Takahashi
,
Yoshihito Suzuki
,
M. Kakihana
2009
Corpus ID: 59497438
Recently our research group has developed a new water-soluble silicon compound. In current work this compound was employed as a…
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Highly Cited
2007
Highly Cited
2007
Evolution and ecological theory: Chance, historical contingency and ecological determinism jointly determine the rate of adaptive radiation
O. Seehausen
Heredity
2007
Corpus ID: 2898068
Evolution and ecological theory: Chance, historical contingency and ecological determinism jointly determine the rate of adaptive…
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2007
2007
Wrinkly-Spreader Fitness in the Two-Dimensional Agar Plate Microcosm: Maladaptation, Compensation and Ecological Success
A. Spiers
PLoS ONE
2007
Corpus ID: 457074
Bacterial adaptation to new environments often leads to the establishment of new genotypes with significantly altered phenotypes…
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Review
2006
Review
2006
Cutis Laxa Type II and Wrinkly Skin Syndrome: Distinct Phenotypes
Neerja Gupta
,
S. Phadke
Pediatric dermatology
2006
Corpus ID: 38692716
Abstract: Cutis laxa is a heterogeneous group of disorders with variable phenotypes and inheritance patterns. Type II cutis laxa…
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1999
1999
Wrinkly Skin Syndrome: Ultrastructural Alterations of the Elastic Fibers
M. D. C. Boente
,
B. Winik
,
R. Asial
Pediatric dermatology
1999
Corpus ID: 41034991
We report the clinical and pathologic features of a patient with wrinkly skin syndrome. The essential clinical features were…
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Review
1993
Review
1993
Del(2q) — cause of the wrinkly skin syndrome?
F. Kreuz
,
Birbei H. Wittwer
Clinical Genetics
1993
Corpus ID: 13451971
We report the cases of a mother and her two sons with de1(2) (q32). Their phenotypes are compared with those of 20 individuals…
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Review
1990
Review
1990
The wrinkly skin syndrome: a report of a case and review of the literature
S. Hurvitz
,
A. Baumgarten
,
R. Goodman
Clinical Genetics
1990
Corpus ID: 2036094
A 2 1/2‐year‐old boy born of Jewish Moroccan parents is reported with physical findings of wrinkled skin on the dorsum of the…
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Review
1987
Review
1987
Wrinkly skin syndrome: Phenotype and additional manifestations
A. C. Casamassima
,
S. Wesson
,
Charles J. Conlon
,
F. Weiss
,
J. M. Opitz
,
J. Reynolds
American journal of medical genetics
1987
Corpus ID: 43407839
The wrinkly skin syndrome is an autosomal recessive disorder characterized by wrinkling of the skin of the dorsum of the hands…
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1983
1983
The wrinkly skin syndrome: A report of two siblings from Saudi Arabia
Z. Karrar
,
A. Elidrissy
,
K. Arabi
,
K. Adam
Clinical Genetics
1983
Corpus ID: 44413878
A brother and sister born to a Saudi couple showed aging appearance, wrinkled skin over the hands and feet, inelastic skin…
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