染色体21q末端缺失综合征一例
出处
《中华医学遗传学杂志》
CAS
CSCD
2002年第4期275-275,共1页
Chinese Journal of Medical Genetics
基金
国家自然科学基金 (3980 0 0 81 )
参考文献5
-
1Theodoropoulos DA,Cowan JM,Elias ER,et al.Physical finding in 21q22 deletion suggest critical region for 21q-phenotype in 22[].American Journal of Medical Genetics.1995
-
2Forster-Gibson CJ,Davies J,MacKenzie JJ,et al.Crytic duplication of 21q in an individual with a clinical diagnosis of Down syndrome[].Clinical Genetics.2001
-
3Sinet PM,Theophile D,Rhamamni Z,et al.Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level[].Biomedicine and Pharmacotherapy.1994
-
4Barlow GM,Chen XN,Shj ZY,et al.Down syndrome congenital heart disease: a narrowed region and a candidated gene[].Genetics Medicine.2001
-
5Yamakawa K,Huot YK,Haendelt MA,et al.DSCAM: a novel member of the immunoglobulin supperfamily maps in a Down syndrome region and is involved in the development of the nervous system[].Human Molecular Genetics.1998
