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MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report
Jae Sun Shim, Kyunghoon Min, Seung Hoon Lee, Ji Eun Park, Sang Hee Park, MinYoung Kim, Sung Han Shim
Ann Rehabil Med. 2015;39(3):482-487.   Published online June 30, 2015
DOI: https://doi.org/10.5535/arm.2015.39.3.482

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MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report
Jae Sun Shim, Kyunghoon Min, Seung Hoon Lee, Ji Eun Park, Sang Hee Park, MinYoung Kim, Sung Han Shim
Annals of Rehabilitation Medicine. 2015;39(3):482   Crossref logo
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8q21.11 Microdeletion syndrome detected by array CGH : A case report
Hae-yeon Park, So Youn Jun, Ah-ra Cho, Joo Hyun Park
European Journal of Paediatric Neurology. 2017;21:e51   Crossref logo
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A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH
Eva Klopocki, Luitgard M. Graul-Neumann, Ulrike Grieben, Holger Tönnies, Hans-Hilger Ropers, Denise Horn, Stefan Mundlos, Reinhard Ullmann
European Journal of Pediatrics. 2007;167(8):903-908   Crossref logo
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The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome
M. Zweier, A. Rauch
Molecular Syndromology. 2011;2(3-5):164-170   Crossref logo
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Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report
Md A Mohd Fadley, Azli Ismail, Thong Meow Keong, Narazah Mohd Yusoff, Zubaidah Zakaria
Journal of Medical Case Reports. 2012;6(1):   Crossref logo
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A Patient with Irritable Bowel Syndrome Improved After Treatment with <italic>Sosiho-tang</italic>, <italic>Jakyakgamcho-tang</italic>, and Acupuncture: A Case Report
Chiho Choi, Seungwon Kwon
The Journal of Internal Korean Medicine. 2022;43(5):960-966   Crossref logo
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Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH
E. Zrnová, V. Vranová, J. Šoukalová, I. Slámová, M. Vilémová, R. Gaillyová, P. Kuglík
Molecular Syndromology. 2011;2(2):88-93   Crossref logo
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Deletion (1)(p32.2-p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?
Milene Mulatinho, Juan Llerena, Trond P. Leren, P. Nagesh Rao, Fabiola Quintero-Rivera
American Journal of Medical Genetics Part A. 2008;146A(17):2284-2290   Crossref logo
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Ventriculitis Associated with Invasive <italic>Klebsiella Pneumoniae</italic> Syndrome: A Case Report
Chai Yoon Kim, Jin Woo Hur, Jeong Gyun Kim, Jong Won Lee, Il-Gyu Yun, Hyun Koo Lee
The Nerve. 2023;9(1):69-74   Crossref logo
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EARLY PHYSICAL THERAPY MEF2C HAPLOID DEFICIENCY SYNDROME (5Q14.3 MICRODELETION)
Eliso Murvanidze
World Science. 2023;(2(80))   Crossref logo
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