These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

314 related articles for article (PubMed ID: 22212331)

  • 1. Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction.
    Lin YH; Chen CP; Chen TC; Hsu CS; Chou SY; Chien SC
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):528-30. PubMed ID: 22212331
    [No Abstract]   [Full Text] [Related]  

  • 2. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP; Su YN; Chen YY; Chern SR; Liu YP; Wu PC; Lee CC; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects.
    Yi Z; Yingjun X; Yongzhen C; Liangying Z; Meijiao S; Baojiang C
    Gene; 2014 Jan; 533(2):565-9. PubMed ID: 24091065
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.
    Çakmaklı S; Çankaya T; Gürsoy S; Koç A; Kırbıyık Ö; Kılıçarslan ÖA; Özer E; Erçal D; Bozkaya ÖG
    Cytogenet Genome Res; 2017; 153(4):175-180. PubMed ID: 29518772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel interstitial deletion of chromosome 2q21.1-q23.3: Case report and literature review.
    Almuzzaini B; Alatwi NS; Alsaif S; Al Balwi MA
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1135. PubMed ID: 31989799
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M; Martinovic J; Sanlaville D; Attié-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
    Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report.
    Sivasankaran S; Ho NK; Knight L
    Ann Acad Med Singap; 1997 Jul; 26(4):507-9. PubMed ID: 9395821
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
    Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
    Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A neonate with the Pelger-Huët anomaly, cleft lip and palate, and agenesis of the corpus callosum, with a chromosomal microdeletion involving 1q41 to 1q42.12.
    Christensen RD; Yaish HM
    J Perinatol; 2012 Mar; 32(3):238-40. PubMed ID: 22370897
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interstitial deletion 2q31 leads to q33.
    Buchanan PD; Rhodes RL; Stevenson CE
    Am J Med Genet; 1983 May; 15(1):121-6. PubMed ID: 6683075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASE.
    Güvenç O; Çimen D; Kaplan MB; Aslan E; Artaç H; Annagür A
    Genet Couns; 2015; 26(4):451-5. PubMed ID: 26852518
    [No Abstract]   [Full Text] [Related]  

  • 12. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.
    Sung PL; Chang CM; Chen CY; Wang PH; Chao KC; Wen KC; Cheng YY; Li YC; Lin CC
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):260-5. PubMed ID: 22795105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation.
    Goumy C; Gay-Bellile M; Salaun G; Kemeny S; Eymard-Pierre E; Biard M; Pebrel-Richard C; Vanlieferinghen P; Francannet C; Tchirkov A; Laurichesse H; Rouzade C; Gouas L; Vago P
    Birth Defects Res A Clin Mol Teratol; 2016 Sep; 106(9):793-7. PubMed ID: 27346851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis.
    Chen YC; Wu WJ; Chang SP; Ma GC; Chen M
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):157-161. PubMed ID: 32039787
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deletion of terminal portion of 6q: report of a case with unusual malformations.
    Shen-Schwarz S; Hill LM; Surti U; Marchese S
    Am J Med Genet; 1989 Jan; 32(1):81-6. PubMed ID: 2705486
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW
    Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
    López I; Bafalliu JA; Bernabé MC; García F; Costa M; Guillén-Navarro E
    Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A fatal autosomal recessive syndrome with multiple congenital contractures].
    Herva R; Leisti J; Kirkinen P; Seppänen U; Martikainen J
    Duodecim; 1985; 101(8):756-62. PubMed ID: 4039655
    [No Abstract]   [Full Text] [Related]  

  • 20. [Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected].
    Picone O; Brisset S; Senat MV; Maurin ML; Frydman R; Tachdjian G
    J Gynecol Obstet Biol Reprod (Paris); 2008 May; 37(3):299-301. PubMed ID: 18160230
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.