WordNet

the act of deleting something written or printed
the omission that is made when an editorial change shortens a written passage; "an editors deletions frequently upset young authors"; "both parties agreed on the excision of the proposed clause" (同)excision, cut
(genetics) the loss or absence of one or more nucleotides from a chromosome
very close or connected in space or time; "contiguous events"; "immediate contact"; "the immediate vicinity"; "the immediate past" (同)immediate
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
informal term for information; "give me the gen on your new line of computers"

PrepTutorEJDIC

削除;〈C〉削除箇所
接触している,隣接する;(…と)隣接している《+『to』(『with』)+『名』》 / (時間的に)前後している
(疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
遺伝子

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1. 先天性の細胞遺伝学的異常 congenital cytogenetic abnormalities
2. ゲノム疾患：概要 genomic disorders an overview
3. 微細欠失症候群（1番～11番染色体） microdeletion syndromes chromosomes 1 to 11
4. 微細欠失症候群（12番～22番染色体） microdeletion syndromes chromosomes 12 to 22
5. X染色体連鎖劣性魚鱗癬 recessive x linked ichthyosis

English Journal

Japanese Journal

Langer-Giedion 症候群に埋伏過剰歯・永久歯萌出遅延・叢生を認めた1例

小児歯科学雑誌 51(4), 467-472, 2013
NAID 130005005951

Unilateral glomerulocystic kidney disease associated with tuberous sclerosis complex in a neonate

Pathology international 62(3), 209-215, 2012-03-01
NAID 10031185191

Molecular Analysis of TSC2/PKD1 Contiguous Gene Deletion Syndrome

The Kobe journal of the medical sciences 57(1), 1-10, 2011
NAID 120003101762

Related Links

Contiguous deletion syndromes - ScienceDirect

Therefore a more appropriate terminology would be 'contiguous deletion syndrome' (CDS), the word 'contiguous' referring to the deletion more than to the genes involved, as disease genes may be interspersed with other genes

Contiguous gene syndrome caused by deletion of 18p11.21 ...

Contiguous gene syndrome caused by deletion of 18p11.21-p11.1 MedGen UID: 762740 • Concept ID: C3549826 • Finding Recent clinical studies Etiology Characterization of 14 novel deletions underlying Rubinstein-Taybi ...

Contiguous Gene Syndrome - an overview | ScienceDirect Topics

Hypotonia-cystinuria syndrome (HCS), formerly known as homozygous 2p16 deletion syndrome, is a recessive contiguous gene syndrome. The disorder is characterized by neonatal and infantile hypotonia and failure to thrive, cystinuria (type 1) and nephrolithiasis, growth hormone deficiency leading to growth retardation, and minor facial dysmorphism ( Jaeken et al., 2006 ).