J. Rips

Orbital nodular fasciitis in child with biallelic germline RBL2 variant.

T. Harel, O. Elpeleg, S. Frenkel, 2022, European journal of medical genetics.

MARS variant associated with both recessive interstitial lung and liver disease and dominant Charcot-Marie-Tooth disease.

T. Harel, A. Antonellis, S. Reif, 2018, European journal of medical genetics.

Establishing a successful HIV counseling and testing service. A blueprint for preventing pediatric HIV infections and translating research into clinical practice.

J. Rips, 1997, Obstetrics and gynecology clinics of North America.

Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening program

S. Almashanu, H. Mandel, A. Luder, 2016, Journal of Inherited Metabolic Disease.

Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected child

T. Harel, V. Meiner, O. Elpeleg, 2020, European Journal of Human Genetics.

Self-Criticism and Self-Compassion: Two sides of the same coin?

J. Rips, 2016 .

De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic features

T. Harel, S. Eventov-Friedman, J. Rips, 2020, American journal of medical genetics. Part A.