D. Kidron

发表

Bi‐allelic IARS mutations in a child with intra‐uterine growth retardation, neonatal cholestasis, and mild developmental delay

M. Muenke, N. Orenstein, K. Weiss, 2017, Clinical genetics.

ARE ALL PHENOTYPICALLY‐NORMAL TURNER SYNDROME FETUSES MOSAICS?

D. Kidron, I. Kedar, A. Amiel, 1996, Prenatal diagnosis.

Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma.

D. Kidron, A. Amiel, M. Fejgin, 2003, Cancer genetics and cytogenetics.

Sonographic Measurements of the Fetal Fastigium Between 20 and 40 Weeks' Gestation

D. Kidron, R. Tepper, R. Hershkovitz, 2009, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Gynecological aspects of female familial dysautonomia.

D. Kidron, O. Sela, C. Maayan, 2000, The Israel Medical Association journal : IMAJ.

Familial lethal skeletal dysplasia with cloverleaf skull and multiple anomalies of brain, eye, face and heart: a new autosomal recessive multiple congenital anomalies syndrome

D. Kidron, A. Amiel, M. Fejgin, 2002, Clinical genetics.

Complete hydatidiform mole and a coexistent viable fetus: report of two cases and review of the literature.

D. Kidron, A. Amiel, M. Fejgin, 2000, Gynecologic oncology.

Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast.

D. Kidron, A. Amiel, M. Fejgin, 2003, Cancer genetics and cytogenetics.

CGH in the detection of confined placental mosaicism (CPM) in placentas of abnormal pregnancies

D. Kidron, A. Amiel, M. Fejgin, 2002, Prenatal diagnosis.

Familial perinatal hemochromatosis: A disease that causes recurrent non-immune hydrops

D. Kidron, D. Kidron, R. Regev, 1999, Journal of perinatal medicine.

Telomere aggregate formation in placenta specimens of pregnancies complicated with pre-eclampsia.

D. Kidron, A. Amiel, M. Fejgin, 2009, Cancer genetics and cytogenetics.

Genetic diagnosis from formalin-fixed fetal tissue using FISH: a new tool for genetic counseling in subsequent pregnancies.

D. Kidron, I. Kedar, A. Amiel, 1996, European journal of obstetrics, gynecology, and reproductive biology.

Fatal kernicterus in a girl deficient in glucose-6-phosphate dehydrogenase: a paradigm of synergistic heterozygosity.

D. Kidron, T. Gelbart, N. Roy‐Chowdhury, 2009, The Journal of pediatrics.

Somatostatin analogue treatment attenuates histological findings of inflammation and increases mRNA expression of interleukin-1 beta in the articular tissues of rats with ongoing adjuvant-induced arthritis

M. Yaron, O. Ziv, D. Kidron, 2005, Rheumatology International.

Transient Cortical Blindness in Preeclampsia With Indication of Generalized Vascular Endothelial Damage

D. Kidron, Anat Kesler, Hagai Kaneti, 1998, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

High incidence of cord entanglement during early pregnancy detected by three-dimensional sonography.

D. Kidron, R. Tepper, R. Hershkovitz, 2009, American journal of perinatology.