M. Werner

发表

Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene

M. Gomori, A. Frumkin, V. Meiner, 2014, neurogenetics.

Cytokine secretion and NK cell activity in human ADAM17 deficiency

O. Mandelboim, Y. Bar-On, Pinchas Tsukerman, 2015, Oncotarget.

Reversed BCR/ABL rearrangement detected by FISH in Philadelphia negative chronic myelocytic leukemia.

S. Ben-Neriah, S. Krichevsky, A. Nagler, 1995, Cancer genetics and cytogenetics.

A human laterality disorder associated with a homozygous WDR16 deletion

A. Frumkin, O. Elpeleg, A. Ta-Shma, 2014, European Journal of Human Genetics.

Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene

M. Gomori, A. Frumkin, V. Meiner, 2014, neurogenetics.

A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis.

J. Schenker, B. Reubinoff, D. Abeliovich, 1998, Human reproduction.

Simultaneous Formation of inv dup(15) and dup(15q) in a Girl with Developmental Delay: Origin of the Abnormal Chromosomes

M. Werner, Dvorah Abeliovich, Judith Dagan, 1995, European journal of human genetics : EJHG.

Intracytoplasmic sperm injection allows fertilization and development of a chromosomally balanced embryo from a binovular zona pellucida.

B. Reubinoff, A. Safran, S. Friedler, 1998, Human reproduction.

Trisomy 18 in a canine thyroid adenoma.

I. Nolte, J. Bullerdiek, U. Bonk, 1996, Cancer genetics and cytogenetics.

Monozygotic multiple gestation after intracytoplasmic sperm injection and preimplantation genetic diagnosis.

H. Daum, S. Yagel, E. Aizenman, 2009, Fertility and sterility.

A patient with Prader–Willi syndrome and a supernumerary marker chromosome r(15)(q11.1‐13p11.1)pat and maternal heterodisomy

I. Lerer, D. Abeliovich, Z. Ben‐Neriah, 2004, American journal of medical genetics. Part A.

The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature.

I. Lerer, B. Sikkema-Raddatz, T. Dijkhuizen, 2009, European journal of medical genetics.

Preimplantation genetic diagnosis for BRCA1/2—a novel clinical experience

M. Werner, E. Girsh, D. Abeliovich, 2009, Prenatal diagnosis.

Endoreduplication and polyploidy in fragile X cells induced by methotrexate and fluorodeoxyuridine: implications for diagnosis.

B. Kerem, C. Kimchi-Sarfaty, T. Schaap, 1991, American journal of medical genetics.