104 related articles for article (PubMed ID: 27264822)
1. [Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion].
Wang H; Wu D; Qin L; Wang T; Zhang H; Xing M; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):361-4. PubMed ID: 27264822
[TBL] [Abstract][Full Text] [Related]
2. [Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].
Wu D; Wang H; Zhang H; Hou Q; Qin L; Wang T; Xiao H; Liao S; Wang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):823-6. PubMed ID: 26663057
[TBL] [Abstract][Full Text] [Related]
3. [Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 18p deletion].
Pan Q; Hu P; Ou J; Jin X; Zhang F; Hu Y; Cheng L; Han L; Ning Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):695-9. PubMed ID: 26418989
[TBL] [Abstract][Full Text] [Related]
4. [Phenotypic and genetic analysis of a child carrying a 17q11.2 microdeletion].
Wang H; Feng Z; Yang K; Gao Y; Huo X; Qin L; Lou G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):695-698. PubMed ID: 28981936
[TBL] [Abstract][Full Text] [Related]
5. [Clinical and genetic analysis of a boy with 9q34.3 microdeletion syndrome].
Wu D; Li T; Wang H; Shi W; Hou Q; Zhang H; Wang T; Yang Y; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):849-852. PubMed ID: 29188614
[TBL] [Abstract][Full Text] [Related]
6. [Phenotypic and genetic analysis of a child featuring multiple malformations due to copy number variation on chromosome 5].
Xue H; Sun X; Lu H; Zhou Y; Guo Y; Zhu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):56-9. PubMed ID: 24510564
[TBL] [Abstract][Full Text] [Related]
7. [Genetic analysis of a child with cleidocranial dysplasia and 6q21-q22.31 microdeletion].
Wu D; Li T; Hou Q; Huo X; Wang X; Wang T; Yang Y; Liu H; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):253-256. PubMed ID: 29653004
[TBL] [Abstract][Full Text] [Related]
8. [A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].
Li H; Chen Y; Li Q; Liu M; Mao J; Song D; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):725-9. PubMed ID: 25449075
[TBL] [Abstract][Full Text] [Related]
9. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
[TBL] [Abstract][Full Text] [Related]
10. [Array comparative genomic hybridization detection of a de novo 4q21.21-q22.1 deletion in a child with severe growth retardation].
Zhou J; Hu P; Liu A; Li L; Ji X; Hui W; Wang Y; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):52-5. PubMed ID: 24510563
[TBL] [Abstract][Full Text] [Related]
11. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
[TBL] [Abstract][Full Text] [Related]
12. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
[TBL] [Abstract][Full Text] [Related]
14. Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.
Papoulidis I; Paspaliaris V; Papageorgiou E; Siomou E; Dagklis T; Sotiriou S; Thomaidis L; Manolakos E
Cytogenet Genome Res; 2015; 145(1):19-24. PubMed ID: 25925190
[TBL] [Abstract][Full Text] [Related]
15. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
Shimojima K; Páez MT; Kurosawa K; Yamamoto T
Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
[TBL] [Abstract][Full Text] [Related]
16. A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.
Wang T; Mao J; Liu MJ; Choy KW; Li HB; Cram DS; Li H; Chen Y
Clin Chim Acta; 2014 Mar; 430():129-33. PubMed ID: 24412318
[TBL] [Abstract][Full Text] [Related]
17. [Phenotypic and genetic analysis of a boy with partial trisomy of 1q].
Wu D; Zhang H; Wang H; Hou Q; Wang T; Li T; Yang Y; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):398-401. PubMed ID: 28604964
[TBL] [Abstract][Full Text] [Related]
18. Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p.
Meschede D; Exeler R; Wittwer B; Horst J
Am J Med Genet; 1998 Dec; 80(5):443-7. PubMed ID: 9880206
[TBL] [Abstract][Full Text] [Related]
19. [Clinical and genetic analysis of a child with chromosomal 13q32.1-q33.3 deletion].
Wang H; Huang C; Li L; Liu Y; Wang T; Zhang Y; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1213-1218. PubMed ID: 31813151
[TBL] [Abstract][Full Text] [Related]
20. [Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion].
Wu D; Shi W; Wang H; Hou Q; Zhang H; Li T; Zhang C; Yang Y; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):718-721. PubMed ID: 28981941
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
