Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature-Reference-Cited by-同舟云学术

Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature

Published:2019-08-27 Issue:10 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Alqahtani Amerh Salem¹²^ORCID,Putoux Audrey¹³⁴,Bonnet Dupeyron Marie Noelle¹⁵,Carneiro Maryline⁶,Lion‐Francois Laurence⁶,Rossi Massimiliano¹⁴^ORCID,Tevissen Hélène⁷,Schluth Bolard Caroline¹³⁴,Labalme Audrey¹,Lesca Gaetan¹³⁴,Till Marianne¹,Edery Patrick¹³⁴,Sanlaville Damien¹³⁴

Affiliation:

1. Department of Medical Genetics, Women Mothers and Children's Hospital Lyon Hospices Civils Lyon France

2. Ministry of Higher Education Riyadh Saudi Arabia

3. Claude Bernard Lyon 1 University Lyon France

4. CRNL, CNRS UMR 5292 INSERM U1028 Lyon France

5. Department of Genetics Valence Hospital's Center Valence France

6. Department of Neuropediatrics, Women Mothers and Children's Hospital Lyon Hospices Civils Lyon France

7. Department of Pediatrics Valence Hospital's Center Valence France

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology