Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations
about
Trisomy 9 mosaicism diagnosed in utero.Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.Constitutional and acquired autosomal aneuploidyPrenatal diagnosis of trisomy 2 mosaicism: a case report.The laboratory-clinician team: a professional call to action to improve communication and collaboration for optimal patient care in chromosomal microarray testingEquine clinical cytogenetics: the past and future.Current knowledge of prenatal diagnosis of mosaic autosomal trisomy in amniocytes: karyotype/phenotype correlations.Rare case of live born with confirmed mosaic trisomy 17 and review of the literature.A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus.Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblasts.Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases.Further observations of true mosaic trisomy 17 ascertained in amniotic fluid cell cultures.Cardiac Failure in a Trisomy 9 Patient Undergoing Anesthesia: A Case ReportThe detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis.The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.Trisomy 3 confined placental mosaicism: a management dilemma.Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case.A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies.
P2860
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P2860
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations
description
1997 nî lūn-bûn
@nan
1997 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մարտին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@ast
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@en
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@nl
type
label
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@ast
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@en
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@nl
prefLabel
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@ast
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@en
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@nl
P2093
P2860
P1433
P1476
Rare trisomy mosaicism diagnos ...... ryotype/phenotype correlations
@en
P2093
A R Brothman
C C Morton
C L Bradshaw
C M Disteche
D Chadwick
D K Kalousek
D L Van Dyke
L G Shaffer
P2860
P304
P356
10.1002/(SICI)1097-0223(199703)17:3<201::AID-PD56>3.0.CO;2-H
P407
P577
1997-03-01T00:00:00Z