Natural history of mosaic trisomy 14 syndrome

scientific article published on September 15, 1992

Natural history of mosaic trisomy 14 syndrome is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1002/AJMG.1320440214
P698PubMed publication ID1456290

P2093author name stringJ. Allanson
A. Fujimoto
C. A. Crowe
M. H. Lipson
V. P. Johnson
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectmosaic trisomy 14Q55785675
trisomyQ844903
P304page(s)189-196
P577publication date1992-09-01
1992-09-15
P1433published inAmerican Journal of Medical Genetics Part AQ15755121
P1476titleNatural history of mosaic trisomy 14 syndrome
P478volume44

Reverse relations

cites work (P2860)
Q50132352A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.
Q73906791Another case of maternal uniparental disomy chromosome 14 syndrome
Q77628884Association of tetralogy of Fallot with a distinct region of del22q11.2.
Q36369918Complete trisomy 14 mosaicism: first live-born case in Korea
Q36128278Congenital ocular anomaly in an infant with trisomy 14 mosaicism
Q24679620Current status of human chromosome 14
Q33922438Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism
Q28245533Lines of Blaschko
Q35194640Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.
Q51962210Mosaic trisomy 15 and hemihypertrophy.
Q38620869Outcome of esophageal atresia/tracheoesophageal fistula in extremely low birth weight neonates (<1000 grams).
Q81502955Partial trisomy 3p and monosomy 7p associated with tetralogy of Fallot and infantile seizure
Q41454160Paternal uniparental disomy for chromosome 14: a case report and review
Q28235463Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations
Q35648570Trisomy 14 mosaicism: a case report and review of the literature

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