31 related articles for article (PubMed ID: 15228573)
1. Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly.
Umlai UI; Haris B; Hussain K; Jithesh PV
Front Endocrinol (Lausanne); 2021; 12():783235. PubMed ID: 35185781
[TBL] [Abstract][Full Text] [Related]
2. Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array.
Zhuang J; Zhang N; Fu W; Yao J; Li Y; Zeng S; Wang Y; Xie Y; Jiang Y
Mol Cytogenet; 2021 Sep; 14(1):46. PubMed ID: 34587985
[TBL] [Abstract][Full Text] [Related]
3. Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation.
Mohamed AM; El-Bassyouni HT; El-Gerzawy AM; Hammad SA; Helmy NA; Kamel AK; Ismail SI; Issa MY; Eid O; Zaki MS
Mol Cytogenet; 2018; 11():57. PubMed ID: 30410579
[TBL] [Abstract][Full Text] [Related]
4. Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.
Yue F; Jiang Y; Yu Y; Yang X; Zhang H; Liu R; Wang R
Medicine (Baltimore); 2018 Nov; 97(45):e13094. PubMed ID: 30407316
[TBL] [Abstract][Full Text] [Related]
5. Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.
Bogs T; Kipfmüller F; Kohlschmidt N; Gembruch U; Müller A; Reutter H
J Med Case Rep; 2016 Mar; 10():76. PubMed ID: 27036947
[TBL] [Abstract][Full Text] [Related]
6. A Saudi Patient with an Interstitial Deletion of Short Arm of Chromosome 3 (p13 to p21) and its Association with Joubert's Syndrome Features.
Mersal AY; Basha MK; Brinji ZS; Avand G
J Clin Neonatol; 2013 Jan; 2(1):46-9. PubMed ID: 24027747
[TBL] [Abstract][Full Text] [Related]
7. Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.
Tosca L; Brisset S; Petit FM; Lecerf L; Rousseau G; Bas C; Laroudie M; Maurin ML; Tapia S; Picone O; Prevot S; Goossens M; Labrune P; Tachdjian G
Eur J Hum Genet; 2010 Aug; 18(8):882-8. PubMed ID: 20424646
[TBL] [Abstract][Full Text] [Related]
8. De novo interstitial duplication 4(q28.1q35) associated with choanal atresia.
Lin S; Kirk EP; McKenzie F; Francis C; Shalhoub C; Turner AM
J Paediatr Child Health; 2004 Jul; 40(7):401-3. PubMed ID: 15228573
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings.
Cakmak-Genc G; Karakas-Celik S; Dursun A; Piskin İE
Gene; 2015 Sep; 568(2):211-4. PubMed ID: 25979671
[TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
[TBL] [Abstract][Full Text] [Related]
11. De novo interstitial tandem duplication of chromosome 4(q21-q28).
Navarro EG; Romero MC; Expósito IL; Velasco CM; Llamas JG; Ramón FJ; Jimenez RD
Am J Med Genet; 1996 Mar; 62(3):297-9. PubMed ID: 8882791
[TBL] [Abstract][Full Text] [Related]
12. Two brothers with Burn-McKeown syndrome.
Wieczorek D; Teber OA; Lohmann D; Gillessen-Kaesbach G
Clin Dysmorphol; 2003 Jul; 12(3):171-4. PubMed ID: 14564154
[TBL] [Abstract][Full Text] [Related]
13. Choanal atresia in a patient with the deletion (9p) syndrome.
Shashi V; Golden WL; Fryburg JS
Am J Med Genet; 1994 Jan; 49(1):88-90. PubMed ID: 8172257
[TBL] [Abstract][Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
