Werner M - Search Results

1

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

Werner M, Ben-Neriah Z, Silverstein S, Lerer I, Dagan Y, Abeliovich D. Werner M, et al. Am J Med Genet A. 2004 Aug 30;129A(2):176-9. doi: 10.1002/ajmg.a.20621. Am J Med Genet A. 2004. PMID: 15316980

2

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

Raas-Rothschild A, Dijkhuizen T, Sikkema-Raddatz B, Werner M, Dagan J, Abeliovich D, Lerer I. Raas-Rothschild A, et al. Among authors: werner m. Eur J Med Genet. 2009 Mar-Jun;52(2-3):140-4. doi: 10.1016/j.ejmg.2009.03.011. Epub 2009 Mar 26. Eur J Med Genet. 2009. PMID: 19328248 Review.

3

Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.

Abeliovich D, Dagan J, Werner M, Lerer I, Shapira Y, Meiner V. Abeliovich D, et al. Among authors: werner m. Eur J Hum Genet. 1995;3(1):49-55. doi: 10.1159/000472273. Eur J Hum Genet. 1995. PMID: 7767656

4

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

Reubinoff BE, Abeliovich D, Werner M, Schenker JG, Safran A, Lewin A. Reubinoff BE, et al. Among authors: werner m. Hum Reprod. 1998 Jul;13(7):1887-92. doi: 10.1093/humrep/13.7.1887. Hum Reprod. 1998. PMID: 9740443

5

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

Abeliovich D, Yehuda O, Krichevsky S, Nagler A, Ben-Neriah S, Werner M, Ludkovsky O, Ben-Yehuda D. Abeliovich D, et al. Among authors: werner m. Cancer Genet Cytogenet. 1995 Jun;81(2):115-7. doi: 10.1016/0165-4608(94)00321-2. Cancer Genet Cytogenet. 1995. PMID: 7621406

6

Preimplantation genetic diagnosis for BRCA1/2--a novel clinical experience.

Sagi M, Weinberg N, Eilat A, Aizenman E, Werner M, Girsh E, Siminovsky Y, Abeliovich D, Peretz T, Simon A, Laufer N. Sagi M, et al. Among authors: werner m. Prenat Diagn. 2009 May;29(5):508-13. doi: 10.1002/pd.2232. Prenat Diagn. 2009. PMID: 19248143

7

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

Kimchi-Sarfaty C, Goitein R, Kerem B, Werner M, Meidan B, Schaap T. Kimchi-Sarfaty C, et al. Among authors: werner m. Am J Med Genet. 1991 Feb-Mar;38(2-3):429-33. doi: 10.1002/ajmg.1320380257. Am J Med Genet. 1991. PMID: 1826810

8

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

Safran A, Reubinoff BE, Porat-Katz A, Werner M, Friedler S, Lewin A. Safran A, et al. Among authors: werner m. Hum Reprod. 1998 Sep;13(9):2575-8. doi: 10.1093/humrep/13.9.2575. Hum Reprod. 1998. PMID: 9806286

9

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

Haimov-Kochman R, Daum H, Lossos F, Aizenman E, Werner M, Yagel S, Laufer N, Simon A, Hurwitz A. Haimov-Kochman R, et al. Among authors: werner m. Fertil Steril. 2009 Dec;92(6):2037.e11-7. doi: 10.1016/j.fertnstert.2009.09.002. Epub 2009 Oct 12. Fertil Steril. 2009. PMID: 19819442 Free article.

10

A human laterality disorder associated with a homozygous WDR16 deletion.

Ta-Shma A, Perles Z, Yaacov B, Werner M, Frumkin A, Rein AJ, Elpeleg O. Ta-Shma A, et al. Among authors: werner m. Eur J Hum Genet. 2015 Sep;23(9):1262-5. doi: 10.1038/ejhg.2014.265. Epub 2014 Dec 3. Eur J Hum Genet. 2015. PMID: 25469542 Free PMC article.

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