| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0003-3995(01)01080-2 |
| P698 | PubMed publication ID | 11694227 |
| P2093 | author name string | Verloes A | |
| Danan C | |||
| Gérard-Blanluet M | |||
| Janaud JC | |||
| Bazin A | |||
| Elbez A | |||
| P2860 | cites work | Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome | Q22253880 |
| Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations | Q28235463 | ||
| Sibs with tetrasomy 18p born to a mother with trisomy 18p. | Q33592881 | ||
| A case of trisomy of chromosome 15 | Q33668606 | ||
| Asymmetry and skin pigmentary anomalies in chromosome mosaicism | Q33674965 | ||
| Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child | Q33678597 | ||
| Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis | Q33678691 | ||
| Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome | Q34142141 | ||
| Natural history of mosaic trisomy 14 syndrome | Q35561391 | ||
| Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review | Q38507572 | ||
| Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism | Q40912476 | ||
| Molecular biology of Beckwith-Wiedemann syndrome | Q41127747 | ||
| Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant | Q41237589 | ||
| True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography | Q41458452 | ||
| Aberrant melanoblast migration associated with trisomy 18 mosaicism | Q41885083 | ||
| Mosaic trisomy 15 found at amniocentesis | Q44069257 | ||
| Trisomy 15 associated with nonimmune hydrops | Q68183223 | ||
| Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata | Q70024579 | ||
| Delineation of a clinical syndrome caused by mosaic trisomy 15 | Q71708137 | ||
| Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15 | Q73134758 | ||
| Prospective prenatal diagnosis of Prader-Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescue | Q73617024 | ||
| Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15 | Q74108606 | ||
| Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literature | Q74744432 | ||
| Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues | Q77482447 | ||
| P433 | issue | 3 | |
| P921 | main subject | mosaic trisomy 15 | Q55785678 |
| P304 | page(s) | 143-148 | |
| P577 | publication date | 2001-07-01 | |
| P1433 | published in | Annales de Génétique | Q26842398 |
| P1476 | title | Mosaic trisomy 15 and hemihypertrophy. | |
| P478 | volume | 44 |
Search more.