scholarly article | Q13442814 |
P2093 | author name string | Taylor JW | |
Kovar IZ | |||
Gilbertson NJ | |||
P2860 | cites work | Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16. | Q33588304 |
Trisomy-16 in a mosaic carrier father and his aborted foetus | Q34633224 | ||
Trisomy of chromosome 16 in a neonate, 47XY,?16+ | Q42096500 | ||
A cytogenetic study of human spontaneous abortions using banding techniques | Q67435369 | ||
TRISOMY OF AUTOSOME 16 | Q76543544 | ||
P433 | issue | 4 Spec No | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | trisomy 16 | Q503642 |
P304 | page(s) | 388-389 | |
P577 | publication date | 1990-04-01 | |
P1433 | published in | Archives of Disease in Childhood | Q4787296 |
P1476 | title | Mosaic trisomy 16 in a live newborn infant | |
P478 | volume | 65 |
Q33678597 | Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child |
Q40982708 | Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases |
Q47371331 | Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature. |
Q33653179 | Prenatal findings in trisomy 16q of paternal origin |
Q28235463 | Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations |
Q73617020 | Severe fetal malformations associated with trisomy 16 confined to the placenta |
Q67545571 | Tissue-specific mosaicism for trisomy 21 and congenital heart disease |
Q71700257 | Trisomy 16 mosaicism in amniotic fluid cell cultures |
Q35194259 | Uniparental disomy for chromosome 16 in humans. |