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Author/Creator Zaidi Mone guestEditor.

1. A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita. Issue 1 (21st August 2018)

Authors:
Khattab, Ahmed; Nelson‐Williams, Carol; Cabreza, Vivienne; Macdonald, Anne; Loring, Erin; Saland, Jeffrey; New, Maria I.
Other Names:
Zaidi Mone guestEditor.
Journal:
Annals of the New York Academy of Sciences
Issue:
Volume 1433:Issue 1(2018)
Page Start:
7
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred. Issue 1 (15th August 2016)

Authors:
Yau, Mabel; Azkawi, Hanan Said Al; Haider, Shozeb; Khattab, Ahmed; Badi, Maryam Al; Abdullah, Wafa; Senani, Aisha Al; Wilson, Robert C.; Yuen, Tony; Zaidi, Mone; New, Maria I.
Other Names:
Zaidi Mone guestEditor.
Journal:
Annals of the New York Academy of Sciences
Issue:
Volume 1376:Issue 1(2016)
Page Start:
65
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype–phenotype nonconcordance. Issue 1 (20th August 2015)

Authors:
Khattab, Ahmed; Yuen, Tony; Al‐Malki, Sultan; Yau, Mabel; Kazmi, Diya; Sun, Li; Harbison, Madeleine; Haider, Shozeb; Zaidi, Mone; New, Maria I.
Other Names:
Zaidi Mone guestEditor.
Journal:
Annals of the New York Academy of Sciences
Issue:
Volume 1364:Issue 1(2016)
Page Start:
5
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗