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Mosaic trisomy 13 and a sacral appendage | BMJ Case Reports
Mosaic trisomy 13 and a sacral appendage | BMJ Case Reports

Mosaic trisomy 22: Report of a patient with normal intelligence - Florez -  2005 - American Journal of Medical Genetics Part A - Wiley Online Library
Mosaic trisomy 22: Report of a patient with normal intelligence - Florez - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library

Should we transfer "mosaic" embryos? - Queensland Family and Fertility  Support
Should we transfer "mosaic" embryos? - Queensland Family and Fertility Support

Allison - Mosaic Trisomy 16
Allison - Mosaic Trisomy 16

High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated  with congenital heart defects and intrauterine growth restriction on fetal  ultrasound - ScienceDirect
High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound - ScienceDirect

Karyotype: mosaic trisomy 13. | Download Scientific Diagram
Karyotype: mosaic trisomy 13. | Download Scientific Diagram

Case report of a pseudo‐isodicentric chromosome 9 resulting in mosaic  trisomy 9 - Beaudry - 2021 - Clinical Case Reports - Wiley Online Library
Case report of a pseudo‐isodicentric chromosome 9 resulting in mosaic trisomy 9 - Beaudry - 2021 - Clinical Case Reports - Wiley Online Library

A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical  description of Warkany-Down syndrome and mechanism of origin - ScienceDirect
A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin - ScienceDirect

Living with Mosaic Trisomy 22 - HubPages
Living with Mosaic Trisomy 22 - HubPages

SciELO - Brasil - New report of two patients with mosaic trisomy 9  presenting unusual features and longer survival New report of two patients  with mosaic trisomy 9 presenting unusual features and longer survival
SciELO - Brasil - New report of two patients with mosaic trisomy 9 presenting unusual features and longer survival New report of two patients with mosaic trisomy 9 presenting unusual features and longer survival

PDF] MOSAIC TRISOMY 22 IN A MALFORMED NEWBORN FEMALE : A NEW CASE |  Semantic Scholar
PDF] MOSAIC TRISOMY 22 IN A MALFORMED NEWBORN FEMALE : A NEW CASE | Semantic Scholar

Brief Clinical Report : Mosaic Trisomy 9 Syndrome With Unusual Phenotype |  Semantic Scholar
Brief Clinical Report : Mosaic Trisomy 9 Syndrome With Unusual Phenotype | Semantic Scholar

4.11 Chromosomal abnormalities | CDC
4.11 Chromosomal abnormalities | CDC

Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature  review - ScienceDirect
Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review - ScienceDirect

Figure 1 from Congenital Ocular Anomaly in an Infant with Trisomy 14  Mosaicism | Semantic Scholar
Figure 1 from Congenital Ocular Anomaly in an Infant with Trisomy 14 Mosaicism | Semantic Scholar

Trisomy 8 mosaicism in adults FTNW.pub - Unique - The Rare ...
Trisomy 8 mosaicism in adults FTNW.pub - Unique - The Rare ...

Finding the Sunshine through Trisomy 14 Mosaicism - Complex Child
Finding the Sunshine through Trisomy 14 Mosaicism - Complex Child

Diagnostics | Free Full-Text | De Novo Mosaic 6p23-p25.3 Tetrasomy Caused  by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p  Phenotype: A Case Report and Literature Review
Diagnostics | Free Full-Text | De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review

Mosaic Trisomy 9 Presenting with Congenital Heart Disease, Facial  Dysmorphism and Pigmentary Skin Lesions: Intricate Issues of Genetic  Counseling | Indian Journal of Pediatrics
Mosaic Trisomy 9 Presenting with Congenital Heart Disease, Facial Dysmorphism and Pigmentary Skin Lesions: Intricate Issues of Genetic Counseling | Indian Journal of Pediatrics

Patient 1: six-year-old boy with mosaic trisomy 9. | Download Scientific  Diagram
Patient 1: six-year-old boy with mosaic trisomy 9. | Download Scientific Diagram

Phenotypic aspects of the patient. The infant at birth (A) and at 12... |  Download Scientific Diagram
Phenotypic aspects of the patient. The infant at birth (A) and at 12... | Download Scientific Diagram

Trisomy 13 (Patau Syndrome): Symptoms, Causes & Outlook
Trisomy 13 (Patau Syndrome): Symptoms, Causes & Outlook

Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9  in a patient with a good prognosis | BMC Medical Genomics | Full Text
Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis | BMC Medical Genomics | Full Text

Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic  analyses. | Semantic Scholar
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses. | Semantic Scholar

My Story - Brandon's Mosaic Trisomy 18 Journey
My Story - Brandon's Mosaic Trisomy 18 Journey

Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell  Lines | Semantic Scholar
Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines | Semantic Scholar

Brandon's Mosaic Trisomy 18 Journey
Brandon's Mosaic Trisomy 18 Journey

Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's  disease in a child with Silver–Russell syndrome | European Journal of Human  Genetics
Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver–Russell syndrome | European Journal of Human Genetics