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Indelman, Margarita
21  results:
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1

The histopathology and phenotypic variability in H syndrome:

Dias‐Polak, David ; Indelman, Margarita ; Bergman, Reuven.
Clinical Case Reports.  6 (2018)  3 - p. 476-478 , 2018
Link: https://doi.org/10.1002/..
 
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2

A case of Netherton syndrome with intestinal atresia, a nov..:

Nevet, Mariela J. ; Indelman, Margarita ; Ben‐Ari, Josef.
International Journal of Dermatology.  56 (2017)  10 - p. 1055-1057 , 2017
Link: https://doi.org/10.1111/..
 
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3

Postzygotic HRAS Mutation Causing Both Keratinocytic Epider..:

Avitan-Hersh, Emily ; Tatur, Sameh ; Indelman, Margarita...
The Journal of Clinical Endocrinology & Metabolism.  99 (2014)  1 - p. E132-E136 , 2014
Link: https://doi.org/10.1210/..
 
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4

Clinico-pathological manifestations of variant late infanti..:

Mandel, Hanna ; Katsanelson, Ksenya Cohen ; Khayat, Morad...
European Journal of Medical Genetics.  57 (2014)  11-12 - p. 607-612 , 2014
Link: https://doi.org/10.1016/..
 
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5

The sound of silence: autosomal recessive congenital ichthy..:

Goldsmith, Tomer ; Fuchs‐Telem, Dana ; Israeli, Shirli...
Experimental Dermatology.  22 (2013)  4 - p. 251-254 , 2013
Link: https://doi.org/10.1111/..
 
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6

A novel nonsense CDH3 mutation in hypotrichosis with juveni..:

Avitan‐Hersh, Emily ; Indelman, Margarita ; Khamaysi, Ziyad..
International Journal of Dermatology.  51 (2012)  3 - p. 325-327 , 2012
Link: https://doi.org/10.1111/..
 
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7

ADULT Syndrome Caused by a Mutation Previously Associated w..:

Avitan-Hersh, Emily ; Indelman, Margarita ; Bergman, Reuven.
Pediatric Dermatology.  27 (2010)  6 - p. 643-645 , 2010
Link: https://doi.org/10.1111/..
 
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8

Disadhesion of epidermal keratinocytes: A histologic clue t..:

Bergman, Reuven ; Hershkovitz, Dov ; Fuchs, Dana...
Journal of the American Academy of Dermatology.  62 (2010)  1 - p. 107-113 , 2010
Link: https://doi.org/10.1016/..
 
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9

A large duplication in LIPH underlies autosomal recessive h..:

Nahum, Sagi ; Pasternack, Sandra M. ; Pforr, Jana...
Archives of Dermatological Research.  301 (2008)  5 - p. 391-393 , 2008
Link: https://doi.org/10.1007/..
 
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10

Rapid detection of homozygous mutations in congenital reces..:

Lugassy, Jennie ; Hennies, Hans Christian ; Indelman, Margarita...
Archives of Dermatological Research.  300 (2007)  2 - p. 81-85 , 2007
Link: https://doi.org/10.1007/..
 
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11

Identification of mutations in the human hairless gene in t..:

Betz, Regina C. ; Indelman, Margarita ; Pforr, Jana...
Archives of Dermatological Research.  299 (2007)  3 - p. 157-161 , 2007
Link: https://doi.org/10.1007/..
 
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12

Homozygosity mapping as a screening tool for the molecular ..:

Mizrachi-Koren, Mordechai ; Shemer, Saar ; Morgan, Michal...
Journal of the American Academy of Dermatology.  55 (2006)  3 - p. 393-401 , 2006
Link: https://doi.org/10.1016/..
 
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13

Hyperphosphatemic familial tumoral calcinosis caused by a m..:

Specktor, Polina ; Cooper, John G. ; Indelman, Margarita.
Journal of Human Genetics.  51 (2006)  5 - p. 487-490 , 2006
Link: https://doi.org/10.1007/..
 
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14

A novel homozygous missense mutation in FGF23 causes Famili..:

Chefetz, Ilana ; Heller, Raoul ; Galli-Tsinopoulou, Assimina...
Human Genetics.  118 (2005)  2 - p. 261-266 , 2005
Link: https://doi.org/10.1007/..
 
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15

Mutations in GALNT3, encoding a protein involved in O-linke..:

Topaz, Orit ; Shurman, Daniel L ; Bergman, Reuven...
Nature Genetics.  36 (2004)  6 - p. 579-581 , 2004
Link: https://doi.org/10.1038/..
 
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