Z. Gelman-Kohan: search on Z-Library

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1

Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis

Iva Toudjarska, Michael W. Kilpatrick, Peter Lembessis, Scott Carra, Gary L. Harton, Michael E. Sisson, Susan H. Black, Harvey J. Stern, Zully Gelman-Kohan, Mordechai Shohat, Petros Tsipouras

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 332 KB

english, 2001

2

Aplasia Cutis Congenita, Elevated Alpha-Fetoprotein, and a Distinct Amniotic Fluid Acetylcholinesterase Electrophoretic Band

Dror, Yigal, Gelman-Kohan, Zulema, Hagai, Zion, Juster-Reicher, Ada, Cohen, Rachel, Mogilner, Benjamin

Journal:

American Journal of Perinatology

Year:

1994

Language:

english

File:

PDF, 682 KB

english, 1994

3

Familial cafe au lait spots: a variant of neurofibromatosis type 1.

Abeliovich, D, Gelman-Kohan, Z, Silverstein, S, Lerer, I, Chemke, J, Merin, S, Zlotogora, J

Journal:

Journal of Medical Genetics

Year:

1995

Language:

english

File:

PDF, 403 KB

english, 1995

4

Correspondence

D. GEVA, T. EZRI, P. SZMUK, Z. GELMAN-KOHAN, B. Z. SHKLAR

Journal:

Pediatric Anesthesia

Year:

1997

Language:

english

File:

PDF, 379 KB

english, 1997

5

The clinical application of spectral karyotyping (SKY™) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs)

Yuval Yaron, Erez Carmon, Myriam Goldstein, Nadia Voskoboinik, Yifat Ochshorn, Zully Gelman-Kohan, Avi Orr-Urtreger

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 175 KB

english, 2003

6

Neurofibromatosis type I (NFI) in Israeli families: Linkage analysis as a diagnostic tool

Segal Elyakim, Israela Lerer, Joel Zlotogora, Michal Sagi, Zully Gelman-Kohan, Saul Merin, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 746 KB

english, 1994

7

Prenatal diagnosis of SLO syndrome

Z. Gelman-Kohan, Dr. J. Chemke

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 65 KB

english, 1995

8

Predictive value of family data for the management of infantile bilateral partial cataract

Oliver, Moshe, Pollack, Ayala, Gelman-Kohan, Zulema, Zalish, Miriam, Hauser, David

Journal:

Year:

1999

Language:

english

File:

PDF, 498 KB

english, 1999

9

Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990–2000

Eliahu G. Stoupel, Helena Frimer, Zvi Appelman, Ziva Ben-Neriah, Hanna Dar, Moshe D. Fejgin, Ruth Gershoni-Baruch, Esther Manor, Gad Barkai, Stavit Shalev, Zully Gelman-Kohan, Orit Reish, Dorit Lev, B

Journal:

International Journal of Biometeorology

Year:

2005

Language:

english

File:

PDF, 248 KB

english, 2005

10

Transcobalamin II deficiency with methylmalonic aciduria in three sisters

H. Bibi, Z. Gelman-Kohan, E. R. Baumgartner, D. S. Rosenblatt

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 66 KB

english, 1999

11

Acrocallosal syndrome: Identification of a novel KIF7 mutation and evidence for oligogenic inheritance

Walsh, Diana M., Shalev, Stavit A., Simpson, Michael A., Morgan, Neil V., Gelman-Kohan, Zulema, Chemke, Juan, Trembath, Richard C., Maher, Eamonn R.

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 470 KB

english, 2013

12

Replication Timing Aberrations and Aneuploidy in Peripheral Blood Lymphocytes of Breast Cancer Patients

Grinberg-Rashi, Helena, Cytron, Samuel, Gelman-Kohan, Zully, Litmanovitch, Talia, Avivi, Lydia

Journal:

Year:

2010

Language:

english

File:

PDF, 558 KB

english, 2010

13

Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit

Lambert van den Heuvel, Wim Ruitenbeek, Roel Smeets, Zully Gelman-Kohan, Orly Elpeleg, Jan Loeffen, Frans Trijbels, Edwin Mariman, Diederik de Bruijn, Jan Smeitink

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 1.34 MB

english, 1998

14

Homozygosity for inversion (2)(p12q14)

Z. Gelman-Kohan, J. Rosensaft, R. Nisani Ben-Cohen, J. Chemke

Journal:

Year:

1993

Language:

english

File:

PDF, 232 KB

english, 1993

15

Human oocytes with Y chromosome can exclude it to the 1st polar body.

I Tur-Kaspa, Y Verlinski, N Gleicher, J Cieslak, S Meltzer, Z Gelman-Kohan

Journal:

Fertility and Sterility

Year:

2001

Language:

english

File:

PDF, 31 KB

english, 2001

16

Further delineation of the acrocallosal syndrome

Z. Gelman-Kohan, J. Antonelli, H. Ankori-Cohen, H. Adar, J. Chemke

Journal:

European Journal of Pediatrics

Year:

1991

Language:

english

File:

PDF, 584 KB

english, 1991

17

CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY

Z. GELMAN-KOHAN, J. ROSENSAFT, H. BEN-HUR, A. HABER, J. CHEMKE

Journal:

Prenatal Diagnosis

Year:

1996

Language:

english

File:

PDF, 338 KB

english, 1996

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