84 related articles for article (PubMed ID: 26153024)
1. Response to "Characteristics of 2p15-p16.1 microdeletion syndrome: review and description of two additional patients".
Ronzoni L; Saletti V; Scuvera G; Esposito S; Milani D
Congenit Anom (Kyoto); 2015 Nov; 55(4):191-2. PubMed ID: 26153024
[No Abstract] [Full Text] [Related]
2. Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients.
Shimojima K; Okamoto N; Yamamoto T
Congenit Anom (Kyoto); 2015 Aug; 55(3):125-32. PubMed ID: 25900130
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15.
Chabchoub E; Vermeesch JR; de Ravel T; de Cock P; Fryns JP
J Med Genet; 2008 Mar; 45(3):189-92. PubMed ID: 18310269
[No Abstract] [Full Text] [Related]
5. Chromosome 2 Microdeletion Syndrome in a Newborn with Amniotic Band Sequence.
Mallett T; McElroy M; Swift K; Reuter S
S D Med; 2018 Apr; 71(4):154-157. PubMed ID: 29996031
[TBL] [Abstract][Full Text] [Related]
6. [Microdeletion 2q23.1 and syndromic findings].
Pérez-Gay L; Gómez-Lado C; Eirís-Puñal J; Dacruz D; Quintela I; Barros-Angueira F; Castro-Gago M
Rev Neurol; 2013 Nov; 57(9):430-1. PubMed ID: 24150955
[No Abstract] [Full Text] [Related]
7. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
Rajcan-Separovic E; Harvard C; Liu X; McGillivray B; Hall JG; Qiao Y; Hurlburt J; Hildebrand J; Mickelson EC; Holden JJ; Lewis ME
J Med Genet; 2007 Apr; 44(4):269-76. PubMed ID: 16963482
[TBL] [Abstract][Full Text] [Related]
8. A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion.
Liang JS; Shimojima K; Ohno K; Sugiura C; Une Y; Ohno K; Yamamoto T
J Med Genet; 2009 Sep; 46(9):645-7. PubMed ID: 19724011
[No Abstract] [Full Text] [Related]
9. Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.
Piccione M; Piro E; Serraino F; Cavani S; Ciccone R; Malacarne M; Pierluigi M; Vitaloni M; Zuffardi O; Corsello G
Eur J Med Genet; 2012 Apr; 55(4):238-44. PubMed ID: 22406401
[TBL] [Abstract][Full Text] [Related]
10. A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome.
Hancarova M; Simandlova M; Drabova J; Mannik K; Kurg A; Sedlacek Z
Am J Med Genet A; 2013 Apr; 161A(4):865-70. PubMed ID: 23495096
[TBL] [Abstract][Full Text] [Related]
11. 2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal Malformation.
Ronzoni L; Novelli A; Brisighelli G; Peron A; Triulzi F; Bianchi V; Leva E; Bedeschi MF
Cytogenet Genome Res; 2016; 150(1):23-28. PubMed ID: 27915340
[TBL] [Abstract][Full Text] [Related]
12. Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15.
Hancarova M; Vejvalkova S; Trkova M; Drabova J; Dleskova A; Vlckova M; Sedlacek Z
Gene; 2013 Mar; 516(1):158-61. PubMed ID: 23266801
[TBL] [Abstract][Full Text] [Related]
13. Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A.
Balci TB; Sawyer SL; Davila J; Humphreys P; Dyment DA
Eur J Med Genet; 2015; 58(6-7):351-4. PubMed ID: 25979662
[TBL] [Abstract][Full Text] [Related]
14. Further characterization of microdeletion syndrome involving 2p15-p16.1.
Félix TM; Petrin AL; Sanseverino MT; Murray JC
Am J Med Genet A; 2010 Oct; 152A(10):2604-8. PubMed ID: 20799320
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic hernia.
Bermudez-Wagner K; Jeng LJ; Slavotinek AM; Sanford EF
Clin Dysmorphol; 2013 Jan; 22(1):22-4. PubMed ID: 23207424
[No Abstract] [Full Text] [Related]
17. 2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.
Dimitrov B; Balikova I; de Ravel T; Van Esch H; De Smedt M; Baten E; Vermeesch JR; Bradinova I; Simeonov E; Devriendt K; Fryns JP; Debeer P
J Med Genet; 2011 Feb; 48(2):98-104. PubMed ID: 21068127
[TBL] [Abstract][Full Text] [Related]
18. Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst.
Hucthagowder V; Liu TC; Paciorkowski AR; Thio LL; Keller MS; Anderson CD; Herman T; Dehner LP; Grange DK; Kulkarni S
Eur J Med Genet; 2012; 55(8-9):485-9. PubMed ID: 22579565
[TBL] [Abstract][Full Text] [Related]
19. Terminal 2q37 deletion and autistic behaviour.
Lukusa T; Smeets E; Vogels A; Vermeesch JR; Fryns JP
Genet Couns; 2005; 16(2):179-80. PubMed ID: 16080299
[No Abstract] [Full Text] [Related]
20. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
