| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-8628(19981228)80:5<473::AID-AJMG7>3.0.CO;2-A |
| P8608 | Fatcat ID | release_mfq72nsc4nb3ni54uuod62pb7m |
| P698 | PubMed publication ID | 9880211 |
| P2093 | author name string | Wang JC | |
| Fischel-Ghodsian N | |||
| Karson EM | |||
| Schreck RR | |||
| Hsu WT | |||
| Falk RE | |||
| Carlson DE | |||
| Bialer MG | |||
| Bhatt SD | |||
| Berry-Kravis E | |||
| Mao R | |||
| Rosenblum-Vos LS | |||
| Garber AP | |||
| Roeder ER | |||
| Hajianpour MJ | |||
| Trunca C | |||
| Leeth EA | |||
| Hux CH | |||
| Linn SK | |||
| Shchepin DA | |||
| P2860 | cites work | Confined placental mosaicism | Q24517911 |
| Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations | Q28235463 | ||
| Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey | Q28248049 | ||
| Trisomy in man | Q28263462 | ||
| Mosaic trisomy 16 in a live newborn infant | Q38364955 | ||
| An audit of trisomy 16 in man. | Q40546787 | ||
| Confined placental mosaicism and stillbirth | Q40741153 | ||
| Variable clinical expression of mosaic trisomy 16 in the newborn infant | Q40768489 | ||
| Uniparental disomy revisited: the first twelve years | Q40841275 | ||
| Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16. | Q41477173 | ||
| Diagnostic testing for Prader-Willi and Angelman syndromes: response | Q43105134 | ||
| Non-mosaic trisomy 16 confined to villi | Q44506854 | ||
| United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis | Q45153294 | ||
| Apparent non-mosaic trisomy 16 in chorionic villi: diagnostic dilemma or clinically significant finding? | Q46307450 | ||
| Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns. | Q52213859 | ||
| Confined placental mosaicism in CVS and pregnancy outcome. | Q54246282 | ||
| Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16 | Q57252335 | ||
| Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker | Q57378051 | ||
| P433 | issue | 5 | |
| P921 | main subject | amniocentesis | Q473768 |
| trisomy 16 | Q503642 | ||
| P304 | page(s) | 473-480 | |
| P577 | publication date | 1998-12-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases | |
| P478 | volume | 80 |
| Q52142100 | An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta. |
| Q54419398 | First trimester detection of trisomy 16 using combined biochemical and ultrasound screening. |
| Q37412801 | Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory |
| Q53410045 | Increased Nuchal Translucency and Early Growth Retardation Related to Confined Placental Mosaicism of Trisomy 16 in a Dichorionic Twin. |
| Q33737626 | Intrauterine growth retardation fetus with trisomy 16 mosaicism |
| Q52164101 | Maternal uniparental disomy of chromosome 16 and body stalk anomaly. |
| Q46949349 | Mosaic trisomy 16: what are the obstetric and long-term childhood outcomes? |
| Q35653039 | Partial trisomy 10 (10q11.2-->pter) and partial trisomy 18 (18p11.2-->pter) associated with abnormal sonographic findings and a maternal serum screen-positive result |
| Q28140943 | Pathogenesis of chromosomal mosaicism and its effect on early human development |
| Q41922048 | Prenatal diagnosis of de novo terminal deletion of chromosome 7q |
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