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The rare 13q33-q34 microdeletions: eight new patients and review of the literature.
Sagi-Dain, Lena; Goldberg, Yael; Peleg, Amir; Sukenik-Halevy, Rivka; Sofrin-Drucker, Efrat; Appelman, Zvi; Josefsberg, Ben Yehoshua Sagi; Ben-Shachar, Shay; Vinkler, Chana; Basel-Salmon, Lina; Maya, Idit.
Affiliation
  • Sagi-Dain L; Genetics Institute, Carmel Medical Center, Affiliated to the Ruth and Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology, 7 Michal St, Haifa, Israel. lena2303@gmail.com.
  • Goldberg Y; Recanati Genetics Institute, Beilinson Hospital, Rabin Medical Center, Petach Tikva, Israel.
  • Peleg A; Genetics Institute, Carmel Medical Center, Affiliated to the Ruth and Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology, 7 Michal St, Haifa, Israel.
  • Sukenik-Halevy R; Recanati Genetics Institute, Beilinson Hospital, Rabin Medical Center, Petach Tikva, Israel.
  • Sofrin-Drucker E; Genetics Institute, Meir Medical Center, Kfar Saba, Israel.
  • Appelman Z; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Josefsberg BYS; National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Ben-Shachar S; Department of Obstetrics and Gynecology, Kaplan Medical Center Rehovot (Affiliated with Hebrew University, Jerusalem), Rehovot, Israel.
  • Vinkler C; Genetics Institute, Kaplan Medical Center, Rehovot, Israel.
  • Basel-Salmon L; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Maya I; Genetics Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Hum Genet ; 138(10): 1145-1153, 2019 Oct.
Article in En | MEDLINE | ID: mdl-31321490
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 13 / Chromosome Deletion / Chromosome Disorders Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Hum Genet Year: 2019 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 13 / Chromosome Deletion / Chromosome Disorders Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Hum Genet Year: 2019 Document type: Article Affiliation country: Country of publication: