Lethal lung hypoplasia and vascular defects in mice with conditional<i>Foxf1</i>overexpression
Avinash V. Dharmadhikari(University of Southern California), Paweł Stankiewicz(Baylor College of Medicine)
Cited by 38
Related Papers
Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
|Journal of Medical Genetics|2009|600
Causal Genetic Variants in Stillbirth
|New England Journal of Medicine|2020|136
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats
|The American Journal of Human Genetics|2004|126
Clinical exome sequencing for inherited retinal degenerations at a tertiary care center
|Scientific Reports|2022|30
Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels
|Genetics in Medicine|2022|24