Genetics in Medicine Open (Jan 2024)
P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome
- Donna McDonald-McGinn,
- Victoria Giunta,
- T. Blaine Crowley,
- Daniel McGinn,
- Lydia Rockart,
- Audrey Green,
- Beverly Emanuel,
- Rosemarie Smith,
- Ellen Moran,
- Maciej Geremek,
- Elaine Zackai,
- Beata Nowakowska
Affiliations
- Donna McDonald-McGinn
- The Children's Hospital of Philadelphia, Perelman School of Medicine of the University of Pennsylvania
- Victoria Giunta
- The Children's Hospital of Philadelphia
- T. Blaine Crowley
- The Children's Hospital of Philadelphia
- Daniel McGinn
- The Children's Hospital of Philadelphia, Perelman School of Medicine of the University of Pennsylvania
- Lydia Rockart
- The Children's Hospital of Philadelphia
- Audrey Green
- The Children's Hospital of Philadelphia
- Beverly Emanuel
- The Children's Hospital of Philadelphia, Perelman School of Medicine of the University of Pennsylvania
- Rosemarie Smith
- Maine Medical Center Portland, ME
- Ellen Moran
- Hassenfeld Children's Hospital at NYU Langone
- Maciej Geremek
- Institute of Mother and Child, Warsaw, Poland
- Elaine Zackai
- The Children's Hospital of Philadelphia, Perelman School of Medicine of the University of Pennsylvania
- Beata Nowakowska
- Institute of Mother and Child, Warsaw, Poland
- Journal volume & issue
-
Vol. 2
p. 101114