المؤلفون: Gowans, LJJ, Cameron-Christie, S, Slayton, RL, Busch, T, Romero-Bustillos, M, Eliason, S, Sweat, M, Sobreira, N, Yu, W, Kantaputra, PN, Wohler, E, Adeyemo, WL, Lachke, SA, Anand, D, Campbell, C, Drummond, BK, Markie, DM, Jansen van Vuuren, WA, Jansen van Vuuren, LJ, Casamassimo, PS, Ettinger, R, Owais, A, van Staden, IP, Amendt, BA, Adeyemo, AA, Murray, JC, Robertson, SP, Butali, A

وصف الملف: text

Relation: https://eprints.whiterose.ac.uk/150243/8/fgene-10-00800.pdf; Gowans, LJJ, Cameron-Christie, S, Slayton, RL et al. (25 more authors) (2019) Missense Pathogenic variants in KIF4A Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus. Frontiers in Genetics, 10. 800. ISSN 1664-8021

الاتاحة: https://eprints.whiterose.ac.uk/150243/
https://eprints.whiterose.ac.uk/150243/8/fgene-10-00800.pdf

المؤلفون: Kantaputra, PN, Paramee, M, Kaewkhampa, A, Hoshino, A, Lees, M, McEntagart, M, Masrour, N, Moore, GE, Pauws, E, Stanier, P

المصدر: J DENT RES , 90 (4) 450 - 455. (2011)

مصطلحات موضوعية: ankyloglossia, cleft lip and palate, dental anomaly, hypodontia, microdontia, TBX22, TRANSCRIPTIONAL REPRESSION, FREQUENT CAUSE, GENE, EXPRESSION, CPX, MALFORMATION, FAMILY, MICE

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/815539/1/815539.pdf; https://discovery.ucl.ac.uk/id/eprint/815539/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/815539/1/815539.pdf
https://discovery.ucl.ac.uk/id/eprint/815539/

المؤلفون: Kantaputra, PN, van den Ouweland, Ans, Sangruchi, T, Limwongse, C

المصدر: Kantaputra , PN , van den Ouweland , A , Sangruchi , T & Limwongse , C 2012 , ' Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation ' , American Journal of Medical Genetics Part A , vol. 158A , no. 7 , pp. 1750-1753 . https://doi.org/10.1002/ajmg.a.35422

مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601, name=EMC MGC-02-96-01

الاتاحة: https://pure.eur.nl/en/publications/6fc4df84-d182-4aae-9631-77520d9e64c2
https://doi.org/10.1002/ajmg.a.35422
http://hdl.handle.net/1765/74074

المؤلفون: Kantaputra, PN, Malaivijitnond, S, Vieira, AR, Heering, J, Dötsch, V, Khankasikum, T, Sripathomsawat, W

وصف الملف: text/plain

Relation: http://d-scholarship.pitt.edu/14345/1/licence.txt; Kantaputra, PN and Malaivijitnond, S and Vieira, AR and Heering, J and Dötsch, V and Khankasikum, T and Sripathomsawat, W (2011) Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate. American Journal of Medical Genetics, Part A, 155 (6). 1432 - 1436. ISSN 1552-4825

الاتاحة: http://d-scholarship.pitt.edu/14345/
http://d-scholarship.pitt.edu/14345/1/licence.txt

المؤلفون: Chan, I, Kivirikko, S, Kantaputra, PN, Irvine, AD, McGrath, JA

المصدر: Chan , I , Kivirikko , S , Kantaputra , PN , Irvine , AD & McGrath , JA 2004 , ' Genotype-phenotype correlation for ectodermal dysplasia syndromes and the tail of p63. ' , Journal of Investigative Dermatology , vol. 123 , no. 2 , 112 , pp. A19 - A19 .

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/5d2b6f32-18ac-46d3-9cf1-35e34892af80

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/5d2b6f32-18ac-46d3-9cf1-35e34892af80

المؤلفون: Kantaputra PN (AUTHOR), Chiewcharnvalijkit K (AUTHOR), Wairatpanich K (AUTHOR), Malikaew P (AUTHOR), Aramrattana A (AUTHOR)

المصدر: Journal of Dentistry for Children. Jan-Apr2007, Vol. 74 Issue 1, p4-9. 6p.

المؤلفون: Gorlin Rj, Kantaputra Pn

المصدر: Clinical Dysmorphology. 1:128

مصطلحات موضوعية: Orthodontics, Hearing loss, business.industry, General Medicine, Overbite, medicine.disease, Pathology and Forensic Medicine, stomatognathic diseases, Dens invaginatus, medicine.anatomical_structure, stomatognathic system, Pediatrics, Perinatology and Child Health, otorhinolaryngologic diseases, Premolar, medicine, Sensorineural hearing loss, Maxillary central incisor, Mandibular lateral incisor, Anatomy, medicine.symptom, business, Genetics (clinical), Anterior teeth

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f1a63d820a3600bf907e97808aa95157
https://doi.org/10.1097/00019605-199207000-00002

المؤلفون: Koster M. I., Payne A. S., Kantaputra P. N., Roop D. R., MARINARI, BARBARA, COSTANZO, ANTONIO

المساهمون: Koster, Mi, Marinari, B, Payne, A, Kantaputra, Pn, Costanzo, A, Roop, Dr

مصطلحات موضوعية: Ankyloblepharon ectodermal dysplasia and clefting, Epidermal differentiation, Skin erosion, TP63, Settore MED/35 - MALATTIE CUTANEE E VENEREE

Relation: info:eu-repo/semantics/altIdentifier/pmid/19681108; info:eu-repo/semantics/altIdentifier/wos/WOS:000269678800011; volume:149; issue:9; firstpage:1942; lastpage:1947; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/2108/34280; info:eu-repo/semantics/altIdentifier/scopus/http://www.scopus.com/inward/record.url?eid=2-s2.0-69249091010&partnerID=40&md5=e649cfc480000c34ed51148f4af2988b

الاتاحة: http://hdl.handle.net/2108/34280
https://doi.org/10.1002/ajmg.a.32794