万方数据
万方数据
万方数据
先天性巨结肠相关疾病和综合征
作者：曹振杰， 陈琦， CAO Zhenjie， CHEN Qi
作者单位：郑州大学医学院第三临床医院小儿外科，河南郑州,450052
刊名：
临床儿科杂志
英文刊名：Journal of Clinical Pediatrics
年，卷(期)：2013,31(1)
被引用次数：4次
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syndrome:SOX10 dysfunction caus different neurocristopathies 1999(09)
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14.Amiel J;Salomon R;Attie T Mutations of the RET-GDNF signaling pathway in Ondine's cur 1996(03)
15.Bolk S;Angrist M;Xie J Endothelin-3 fram魔鬼英语
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16.Hayes CE;Kawatu D;Mangray S Rectal suction biopsy to exclude the diagnosis of hirschsprungdia 2012(03)
17.Merkler RG;Solish SB;Scherzer AL Meningomyelocele and Hirschprung dia:theoretical and clinical significance 1985(02)
18.Claun N;Andersson P;Tommerup N Familial occurrence of neuroblastoma,von Recklinghaun's
neurofibromatosis,Hirschsprung'sagangliosis and jaw-winking syndrome 1989(05)
19.Murphy HR;Carver M J;Brooks AS Two brothers with Goldberg-Shprintzensyndrome 20使失望英语
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20.Hurst JA;Markiewicz M;Kumar D Unknown syndrome:Hirschsprung's dia现任广州市市长
,microcephaly,and iris coloboma:a new syndrome of defective neuronal migration 1988(07)
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a ca for fetoscopy 1975(04)
24.Al-Gazali LI;Donnai D;Mueller RF Hirschsprung's dia,hypoplastic nails,and minor dysmorphic features:a
distinct autosomal recessive syndrome 1988(11)
25.Huang T;Elias ER;Mulliken JB A new syndrome:heart defect,laryngeal anomalies,preaxialpolydactyly,and colonic aganglionosis in sibs 1999(03)
26.Reynolds JF;Barber JC;Alford BA Familial Hirschsprung's dia and type D brachydactyly:a report of four affected males in two generations 1983(02)
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28.Reish O;Gorlin R J;Hordinsky M Brain anomalies,retardation of mentality and growth,ectodermal
dysplasia,skeletal malformations,Hirschsprung dia,ear deformity and deafness,eye hypoplasia,cleft
palate,cryptorchidism,and kidney dysplasia/hypoplasia(BRESEK/BRESHECK):new X-linked syndrome 1997(04)
29.Hall CM Werner's mesomelic dysplasia with ventricular ptal defect and Hirschsprung's dia 1981(04)
30.Davenport M;Taitz LS;Dickson JA The Kaufman-McKusick syndrome:another association 1989(11)
31.Stone DL;Slavotinek A;Bouffard GG;Banerjee Basu-S;Baxevanis AD;Barr M;Biecker LG Mutation of a gene encoding
a putative chaperonin caus McKusick-Kaufman syndrome.[外文期刊] 2000(1)
32.Slavotinek AM;Stone EM;Mykytyn K Mutations in MKKS cau Bardet-Biedl syndrome 2000(01)
33.Waterham HR;Wijburg FA;Hennekam RC Smith-Lemli-Opitz syndrome is caud by mutations in the 7-dehydrocholesterol reducta gene 1998(02)
34.Patterson K;Toomey KE;Chandra RS Hirschsprung dia in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome 1983(03)
35.Makitie O;Kaitila I Cartilage-hair hypoplasia-clinical manifestations in 108 Finnish patients 1993(03)
36.Sulisalo T;Sistonen P;Hastbacka J Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis 1993(04)
37.Mandel H;Brik R;Ludatscher R Congenital muscular dystrophy with neurological abnormalities:association with Hirschsprung dia 1993(01)
38.Kim JJ;Armstrong DD;Fishman MA Multicore myopathy大学生必读书目
,microcephaly,aganglionosis,and short stature 1994(03)
39.Mallory SB;Haynie LS;Williams ML Ichthyosis,deafness,and Hirschsprung's dia 1989(01)
40.Kaplan P X linked recessive inheritance of agenesis of the corpus callosum 1983(02)
41.Okamoto N;Wada Y;Goto M Hydrocephalus and Hirschsprung's dia in a patient with a mutation of L1CAM 1997(08)
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引用本文格式老人与海书评
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