109 related articles for article (PubMed ID: 24107884)
1. [Clinical and genetic analysis of idiopathic intellectual disability based on array comparative genomic hybridization].
Kashevarova AA; Skryabin NA; Cheremnykh AD; Tolmacheva EN; Sazhenova EA; Salyukova OA; Chechetkina NN; Didenko LI; Sukhanova NN; Yakovleva YS; Torkhova NB; Nazarenko LP; Magini P; Graziano C; Romeo G; Lebedev IN
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(9):70-4. PubMed ID: 24107884
[TBL] [Abstract][Full Text] [Related]
2. Array CGH analysis of a cohort of Russian patients with intellectual disability.
Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
[TBL] [Abstract][Full Text] [Related]
3. The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.
Bartnik M; Wiśniowiecka-Kowalnik B; Nowakowska B; Smyk M; Kędzior M; Sobecka K; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Castañeda J; Własienko P; Bezniakow N; Obersztyn E; Bocian E
Dev Period Med; 2014; 18(3):307-17. PubMed ID: 25182394
[TBL] [Abstract][Full Text] [Related]
4. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
[TBL] [Abstract][Full Text] [Related]
5. Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patients.
Siggberg L; Ala-Mello S; Jaakkola E; Kuusinen E; Schuit R; Kohlhase J; Böhm D; Ignatius J; Knuutila S
Am J Med Genet A; 2010 Jun; 152A(6):1398-410. PubMed ID: 20503314
[TBL] [Abstract][Full Text] [Related]
6. The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
D'Arrigo S; Gavazzi F; Alfei E; Zuffardi O; Montomoli C; Corso B; Buzzi E; Sciacca FL; Bulgheroni S; Riva D; Pantaleoni C
J Child Neurol; 2016 May; 31(6):691-9. PubMed ID: 26511719
[TBL] [Abstract][Full Text] [Related]
7. Application of array-based comparative genome hybridization in children with developmental delay or mental retardation.
Liang JS; Shimojima K; Yamamoto T
Pediatr Neonatol; 2008 Dec; 49(6):213-7. PubMed ID: 19166117
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.
Debost-Legrand A; Capri Y; Gouas L; Pebrel-Richard C; Veronese L; Tchirkov A; Haoud K; Boespflug-Tanguy O; Goumy C; Vago P
Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667
[TBL] [Abstract][Full Text] [Related]
10. Microdeletion and microduplication syndromes.
Vissers LE; Stankiewicz P
Methods Mol Biol; 2012; 838():29-75. PubMed ID: 22228006
[TBL] [Abstract][Full Text] [Related]
11. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
He XY; Chen XC; Li R; Li P; Lu AM
Zhongguo Dang Dai Er Ke Za Zhi; 2015 May; 17(5):459-63. PubMed ID: 26014695
[TBL] [Abstract][Full Text] [Related]
12. Analysis of chromosomal aberrations in patients with mental retardation using the array-CGH technique: a single Czech centre experience.
Zrnová E; Vranová V; Slámová I; Gaillyová R; Kuglík P
Folia Biol (Praha); 2011; 57(5):206-15. PubMed ID: 22123463
[TBL] [Abstract][Full Text] [Related]
13. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T
Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989
[TBL] [Abstract][Full Text] [Related]
14. Array-based comparative genome hybridization in clinical genetics.
Bar-Shira A; Rosner G; Rosner S; Goldstein M; Orr-Urtreger A
Pediatr Res; 2006 Sep; 60(3):353-8. PubMed ID: 16857771
[TBL] [Abstract][Full Text] [Related]
15. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F
Arch Neurol; 2012 Mar; 69(3):322-30. PubMed ID: 22083797
[TBL] [Abstract][Full Text] [Related]
16. What can we learn from old microdeletion syndromes using array-CGH screening?
Mosca-Boidron AL; Bouquillon S; Faivre L; Callier P; Andrieux J; Marle N; Bonnet C; Vincent-Delorme C; Berri M; Plessis G; Manouvrier-Hanu S; Dieux-Coeslier A; Thauvin-Robinet C; Pipiras E; Delahaye A; Payet M; Ragon C; Masurel-Paulet A; Questiaux E; Benzacken B; Jonveaux P; Mugneret F; Holder-Espinasse M
Clin Genet; 2012 Jul; 82(1):41-7. PubMed ID: 21722100
[TBL] [Abstract][Full Text] [Related]
17. Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
Nicholl J; Waters W; Mulley JC; Suwalski S; Brown S; Hull Y; Barnett C; Haan E; Thompson EM; Liebelt J; Mcgregor L; Harbord MG; Entwistle J; Munt C; White D; Chitti A; Baulderstone D; Ketteridge D; ; Friend K; Bain SM; Yu S
Pathology; 2014 Jan; 46(1):41-5. PubMed ID: 24300712
[TBL] [Abstract][Full Text] [Related]
18. Clinical utility of an array comparative genomic hybridization analysis for Williams syndrome.
Yagihashi T; Torii C; Takahashi R; Omori M; Kosaki R; Yoshihashi H; Ihara M; Minagawa-Kawai Y; Yamamoto J; Takahashi T; Kosaki K
Congenit Anom (Kyoto); 2014 Nov; 54(4):225-7. PubMed ID: 24853877
[TBL] [Abstract][Full Text] [Related]
19. 15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Vanlerberghe C; Petit F; Malan V; Vincent-Delorme C; Bouquillon S; Boute O; Holder-Espinasse M; Delobel B; Duban B; Vallee L; Cuisset JM; Lemaitre MP; Vantyghem MC; Pigeyre M; Lanco-Dosen S; Plessis G; Gerard M; Decamp M; Mathieu M; Morin G; Jedraszak G; Bilan F; Gilbert-Dussardier B; Fauvert D; Roume J; Cormier-Daire V; Caumes R; Puechberty J; Genevieve D; Sarda P; Pinson L; Blanchet P; Lemeur N; Sheth F; Manouvrier-Hanu S; Andrieux J
Eur J Med Genet; 2015 Mar; 58(3):140-7. PubMed ID: 25596525
[TBL] [Abstract][Full Text] [Related]
20. Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability.
Moeschler JB
Curr Opin Neurol; 2008 Apr; 21(2):117-22. PubMed ID: 18317267
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
