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12q24.11
A chromosome band present on 12q
National Institutes of Health
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Related topics
Related topics
3 relations
12q
ATP2A2 wt Allele
Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Myosin 1H and the soft tissue profile of african american females with mandibular prognathism
John M. Burnheimer
,
K. Deeley
,
A. R. Vieira
Rio de Janeiro Dental Journal (Revista Científica…
2019
Corpus ID: 209260388
Introduction: The aim of this study was to explore the influence of Myosin 1H on the soft tissue profile of African American…
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2018
2018
A preliminary study on MYO1H single nucleotide polymorphism (rs10850110) in mandibular prognathism in Malay population
S. Yahya
,
Nurul Syafiqah Abdul Razak
,
Noraini Abu Bakar
2018
Corpus ID: 141067050
Evidence suggests that several genes; including Myo1H, play an important role in the etiology of Class III malocclusion. Single…
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2018
2018
Genomic Profile and Pathologic Features of Diffuse Large B-Cell Lymphoma Subtype of Methotrexate-associated Lymphoproliferative Disorder in Rheumatoid Arthritis Patients
J. Carreras
,
Yara Yukie Kikuti
,
+11 authors
N. Nakamura
American Journal of Surgical Pathology
2018
Corpus ID: 13697501
Rheumatoid arthritis patients often develop the diffuse large B-cell lymphoma subtype of methotrexate-associated…
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2015
2015
[Metatropic dysplasia in a girl with c.1811_1812delinsAT mutation in exon 11 of the TRPV4 gene not previously reported].
F. Cammarata-Scalisi
,
U. Matysiak-Scholze
,
+4 authors
Yudith Guerrero
Archivos Argentinos de Pediatria
2015
Corpus ID: 42990600
Metatropic dysplasia is a skeletal disorder with clinical heterogeneity, characterized by craniofacial dysmorphy including…
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2013
2013
Backtracking Of The Genetic Events Preceding Acute Leukemia Diagnosis
O. Zimmermannová
,
M. Žaliová
,
+13 authors
J. Zuna
2013
Corpus ID: 208484112
In contrast to the precise monitoring of the dynamics of the leukemic clone after diagnosis, little is known about the presence…
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2011
2011
Clinical, laboratory, and genetic studies of families with Charcot-Marie-Tooth type 2C disease
G. Landouré
2011
Corpus ID: 81591233
Charcot-Marie-Tooth disease type 2C (CMT2C) is an autosomal dominant neuropathy characterized by limb, diaphragm, and laryngeal…
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