215 related articles for article (PubMed ID: 28085742)
1. Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome.
Ozcan A; Acer H; Ciraci S; Gumus H; Karakukcu M; Patiroglu T; Ozdemir MA; Unal E
J Pediatr Hematol Oncol; 2017 May; 39(4):e224-e226. PubMed ID: 28085742
[TBL] [Abstract][Full Text] [Related]
2. Hip displacement in Wolf-Hirschhorn syndrome: Report on three cases and review of associated musculoskeletal pathologies.
Buddhdev PK; Sabir A; Kokkinakis M; Irving M; Norman-Taylor F
Am J Med Genet A; 2020 Jun; 182(6):1449-1453. PubMed ID: 32259397
[TBL] [Abstract][Full Text] [Related]
3. Interstitial microdeletion of 4p16.3: contribution of WHSC1 haploinsufficiency to the pathogenesis of developmental delay in Wolf-Hirschhorn syndrome.
Izumi K; Okuno H; Maeyama K; Sato S; Yamamoto T; Torii C; Kosaki R; Takahashi T; Kosaki K
Am J Med Genet A; 2010 Apr; 152A(4):1028-32. PubMed ID: 20358621
[No Abstract] [Full Text] [Related]
4. 109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.
Okamoto N; Ohmachi K; Shimada S; Shimojima K; Yamamoto T
Am J Med Genet A; 2013 Jun; 161A(6):1465-9. PubMed ID: 23637096
[TBL] [Abstract][Full Text] [Related]
5. Wolf-Hirschhorn syndrome: A case series from India.
Chaudhry C; Kaur A; Panigrahi I; Kaur A
Am J Med Genet A; 2020 Dec; 182(12):3048-3051. PubMed ID: 32914558
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
Finzi S; Pinto CF; Wiggs JL
Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648
[TBL] [Abstract][Full Text] [Related]
7. Wolf-Hirschhorn syndrome.
Akhtar N
J Coll Physicians Surg Pak; 2008 Apr; 18(4):254-6. PubMed ID: 18474167
[TBL] [Abstract][Full Text] [Related]
8. A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome.
Zorlu P; Eksioglu AS; Ozkan M; Tos T; Senel S
Genet Couns; 2014; 25(3):299-303. PubMed ID: 25365852
[TBL] [Abstract][Full Text] [Related]
9. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
Battaglia A; Filippi T; Carey JC
Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):246-51. PubMed ID: 18932224
[TBL] [Abstract][Full Text] [Related]
10. Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.
Hannes F; Drozniewska M; Vermeesch JR; Haus O
Eur J Med Genet; 2010; 53(3):136-40. PubMed ID: 20197130
[TBL] [Abstract][Full Text] [Related]
11. Pediatric diagnosis not made until adulthood: a case of Wolf-Hirschhorn syndrome.
Coppola A; Chinthapalli K; Hammond P; Sander JW; Sisodiya SM
Gene; 2013 Jan; 512(2):532-5. PubMed ID: 23064045
[TBL] [Abstract][Full Text] [Related]
12. Wolf-Hirschhorn syndrome: a case study and disease overview.
Bailey R
Adv Neonatal Care; 2014 Oct; 14(5):318-21. PubMed ID: 25137600
[TBL] [Abstract][Full Text] [Related]
13. Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.
Dai Y; Yang J; Chen Y; Bao L; Cheng Q
Pediatr Int; 2013 Jun; 55(3):368-70. PubMed ID: 23782367
[TBL] [Abstract][Full Text] [Related]
14. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
Yang WX; Pan H; Wang ST; Li L; Wu HR; Qi Y
Taiwan J Obstet Gynecol; 2016 Feb; 55(1):104-8. PubMed ID: 26927259
[TBL] [Abstract][Full Text] [Related]
15. A practical approach to dental care for patients with Wolf-Hirschhorn syndrome.
Serrano Martín C; Fernández Feijoo J; García Mato E; Varela Aneiros I; Diniz Freitas M; Vázquez García E; Limeres Posse J
Spec Care Dentist; 2022 Mar; 42(2):137-142. PubMed ID: 34538003
[TBL] [Abstract][Full Text] [Related]
16. Clinical features in adult patient with Wolf-Hirschhorn syndrome.
Martínez-Quintana E; Rodríguez-González F
Morphologie; 2014 Jun; 98(321):86-9. PubMed ID: 24656633
[TBL] [Abstract][Full Text] [Related]
17. A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome.
Terrone G; Cappuccio G; Genesio R; Esposito A; Fiorentino V; Riccitelli M; Nitsch L; Brunetti-Pierri N; Del Giudice E
Am J Med Genet A; 2014 Jan; 164A(1):190-3. PubMed ID: 24243641
[TBL] [Abstract][Full Text] [Related]
18. Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review.
Paprocka J; Kaminiów K; Yetkin O; Tekturk P; Baykan B; Leiz S; Kluger G; Striano P
Seizure; 2024 Mar; 116():14-23. PubMed ID: 36526544
[TBL] [Abstract][Full Text] [Related]
19. Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).
Saberi A; Shariati G; Hamid M; Galehdari H; Abdorasouli N
Arch Iran Med; 2014 Sep; 17(9):642-4. PubMed ID: 25204484
[TBL] [Abstract][Full Text] [Related]
20. From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature.
Wiel LC; Bruno I; Barbi E; Sirchia F
Ital J Pediatr; 2022 May; 48(1):72. PubMed ID: 35550183
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]