Author/Creator: Ebrahim, Salah - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Ebrahim, Salah

1. Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay. Issue 7 (3rd April 2014)

Authors:: Prasun, Pankaj; Hankerd, Michael; Kristofice, Melissa; Scussel, Lindsey; Sivaswamy, Lalitha; Ebrahim, Salah
Journal:: American journal of medical genetics
Issue:: Volume 164:Issue 7(2014.)
Page Start:: 1815
Record Type:: Journal Article
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2. Genomic detection of a familial 382 Kb 6q27 deletion in a fetus with isolated severe ventriculomegaly and her affected mother. Issue 9 (8th September 2018)

Authors:: Thakur, Mili; Bronshtein, Elena; Hankerd, Michael; Adekola, Henry; Puder, Karoline; Gonik, Bernard; Ebrahim, Salah
Journal:: American journal of medical genetics
Issue:: Volume 176:Issue 9(2018)
Page Start:: 1985
Record Type:: Journal Article
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3. Prenatal Lethal Diagnosis of 8p23.1 Duplication Syndrome Associated with Omphalocele and Encephalocele. (25th February 2023)

Authors:: Hicks, Melissa A.; Ebrahim, Salah; Gonik, Bernard
Other Names:: Mittal Balraj Academic Editor.
Journal:: Case reports in genetics
Issue:: Volume 2023(2023)
Page Start:
Record Type:: Journal Article
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4. Use of Fluorescence In Situ Hybridization Technology to Explain a Confusing Case of Vasa Previa. (24th July 2017)

Authors:: Alhousseini, Ali; Ebrahim, Salah; Awadalla, Michael; Patwardhan, Manasi; Gonik, Bernard
Journal:: Journal of ultrasound in medicine
Issue:: Volume 37:Number 1(2018)
Page Start:: 305
Record Type:: Journal Article
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