Author/Creator: Jones, Gabriela E. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Jones, Gabriela E.

1. 14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disability. (2nd July 2016)

Authors:: Jones, Gabriela E.; Robertson, Lisa; Warman, Paul; Craft, Emily V.; Cresswell, Lara; Vasudevan, Pradeep C.
Journal:: Ophthalmic genetics
Issue:: Volume 37:Number 3(2016)
Page Start:: 352
Record Type:: Journal Article
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2. Microform holoprosencephaly with bilateral congenital elbow dislocation; increasing the phenotypic spectrum of Steinfeld syndrome. Issue 3 (5th January 2016)

Authors:: Jones, Gabriela E.; Robertson, Lisa; Maniyar, Amit; Shammas, Christos; Phelan, Marie M.; Vasudevan, Pradeep C.; Tanteles, George A.
Journal:: American journal of medical genetics
Issue:: Volume 170:Issue 3(2016)
Page Start:: 754
Record Type:: Journal Article
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3. Renal anomalies and lymphedema distichiasis syndrome. A rare association?. Issue 8 (23rd May 2017)

Authors:: Jones, Gabriela E.; Richmond, Anna K.; Navti, Osric; Mousa, Hatem A.; Abbs, Stephen; Thompson, Edward; Mansour, Sahar; Vasudevan, Pradeep C.
Journal:: American journal of medical genetics
Issue:: Volume 173:Issue 8(2017)
Page Start:: 2251
Record Type:: Journal Article
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4. Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature. (9th November 2015)

Authors:: Jones, Gabriela E.; Mousa, Hatem A.; Rowley, Helen; Houtman, Peter; Vasudevan, Pradeep C.
Journal:: Prenatal diagnosis
Issue:: Volume 35:Number 13(2015:Dec.)
Page Start:: 1336
Record Type:: Journal Article
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