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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/04/18 23:52:13」(JST)

English Journal

Dasouki M, Andrews B, Parimi P, Kamnasaran D.SourceDepartment of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas. mdasouki@kumc.edu.
American journal of medical genetics. Part A.Am J Med Genet A.2013 Feb 26. doi: 10.1002/ajmg.a.35879. [Epub ahead of print]
Agnathia-otocephaly is a rare craniofacial malformation complex that is caused by de novo heterozygous and biallelic mutations in PRRX1 in two unrelated babies, respectively. We studied the PRRX1 gene in a non-consanguineous Indonesian female infant who was diagnosed prenatally with severe retrognat
PMID 23444262

Geometric morphometric analysis of craniofacial variation, ontogeny and modularity in a cross-sectional sample of modern humans.

Wellens HL, Kuijpers-Jagtman AM, Halazonetis DJ.SourceDepartment of Orthodontics and Craniofacial Biology, Radboud University Nijmegen, Medical Centre Nijmegen, Nijmegen, The Netherlands.
Journal of anatomy.J Anat.2013 Feb 21. doi: 10.1111/joa.12027. [Epub ahead of print]
This investigation aimed to quantify craniofacial variation in a sample of modern humans. In all, 187 consecutive orthodontic patients were collected, of which 79 were male (mean age 13.3, SD 3.7, range 7.5-40.8) and 99 were female (mean age 12.3, SD 1.9, range 8.7-19.1). The male and female subgrou
PMID 23425043

Fagerberg CR, Graakjaer J, Heinl UD, Ousager LB, Dreyer I, Kirchhoff M, Rasmussen AA, Lautrup CK, Birkebaek N, Sorensen K.SourceDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark. Electronic address: christina.fagerberg@ouh.regionsyddanmark.dk.
European journal of medical genetics.Eur J Med Genet.2013 Feb;56(2):98-107. doi: 10.1016/j.ejmg.2012.09.009. Epub 2012 Oct 10.
22q11.2 distal deletion syndrome is distinct from the common 22q11.2 deletion syndrome and caused by microdeletions localized adjacent to the common 22q11 deletion at its telomeric end. Most distal deletions of 22q11 extend from LCR22-4 to an LCR in the range LCR22-5 to LCR22-8. We present three pat
PMID 23063575

宮地斉,黒柳範雄,落合栄樹,神谷昇,下郷和雄
日本口腔外科学会雑誌 60(6), 375-379, 2014
… A 21-year-old woman presented with maxillary protrusion and a gummy smile along with mandibular retrognathism. …
NAID 130005083479

伊集院公美子,渋澤龍之,藤川泰成,新真紀子,槇宏太郎
日本顎変形症学会雑誌 24(1), 1-8, 2014
… Although mandibular retrognathism has been reported particularly frequently, no reports have addressed acquired facial deformity of patients with mandibular prognathism. …
NAID 130003397165

Maxillary stability after Le Fort I osteotomy with self-setting α-tricalcium phosphate and an absorbable plate

Ueki Koichiro,Okabe Katsuhiko,Marukawa Kohei,Mukozawa Aya,Moroi Akinori,Miyazaki Mao,Sotobori Megumi,Ishihara Yuri,Yoshizawa Kunio,Ooi Kazuhiro,Kawashiri Shuichi
International Journal of Oral and Maxillofacial Surgery 42(5), 597-607, 2013-03
… Subjects comprised 45 patients diagnosed with mandibular prognathism with maxillary retrognathism and mandibular prognathism with bimaxillary asymmetry. …
NAID 120005253211