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Author/Creator Hu, Tommy

1. Cornelia de Lange syndrome in diverse populations. Issue 2 (6th January 2019)

Authors:
Dowsett, Leah; Porras, Antonio R.; Kruszka, Paul; Davis, Brandon; Hu, Tommy; Honey, Engela; Badoe, Eben; Thong, Meow‐Keong; Leon, Eyby; Girisha, Katta M.; Shukla, Anju; Nayak, Shalini S.; Shotelersuk, Vorasuk; Megarbane, Andre; Phadke, Shubha; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Ferr...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 2(2019)
Page Start:
150
Record Type:
Journal Article
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2. Cornelia de Lange syndrome in diverse populations. Issue 2 (6th January 2019)

Authors:
Dowsett, Leah; Porras, Antonio R.; Kruszka, Paul; Davis, Brandon; Hu, Tommy; Honey, Engela; Badoe, Eben; Thong, Meow‐Keong; Leon, Eyby; Girisha, Katta M.; Shukla, Anju; Nayak, Shalini S.; Shotelersuk, Vorasuk; Megarbane, Andre; Phadke, Shubha; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Ferr...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 2(2019)
Page Start:
150
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Cover Image, Volume 176A, Number 5, May 2018. Issue 5 (21st April 2018)

Authors:
Kruszka, Paul; Porras, Antonio R.; de Souza, Deise Helena; Moresco, Angélica; Huckstadt, Victoria; Gill, Ashleigh D.; Boyle, Alec P.; Hu, Tommy; Addissie, Yonit A.; Mok, Gary T. K.; Tekendo‐Ngongang, Cedrik; Fieggen, Karen; Prijoles, Eloise J.; Tanpaiboon, Pranoot; Honey, Engela; Luk, Ho‐Ming; Lo...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. Issue 2 (24th July 2018)

Authors:
Hu, Tommy; Kruszka, Paul; Martinez, Ariel F.; Ming, Jeffrey E.; Shabason, Emily K.; Raam, Manu S.; Shaikh, Tamim H.; Pineda‐Alvarez, Daniel E.; Muenke, Maximilian
Other Names:
Kruszka Paul S. guestEditor.; Solomon Benjamin D. guestEditor.; Muenke Maximilian guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 178:Issue 2(2018)
Page Start:
175
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Phenotype delineation of ZNF462 related syndrome. Issue 10 (30th July 2019)

Authors:
Kruszka, Paul; Hu, Tommy; Hong, Sungkook; Signer, Rebecca; Cogné, Benjamin; Isidor, Betrand; Mazzola, Sarah E.; Giltay, Jacques C.; van Gassen, Koen L. I.; England, Eleina M.; Pais, Lynn; Ockeloen, Charlotte W.; Sanchez‐Lara, Pedro A.; Kinning, Esther; Adams, Darius J.; Treat, Kayla; Torres‐Marti...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 10(2019)
Page Start:
2075
Record Type:
Journal Article
View Content:
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8. Williams–Beuren syndrome in diverse populations. Issue 5 (21st April 2018)

Authors:
Kruszka, Paul; Porras, Antonio R.; de Souza, Deise Helena; Moresco, Angélica; Huckstadt, Victoria; Gill, Ashleigh D.; Boyle, Alec P.; Hu, Tommy; Addissie, Yonit A.; Mok, Gary T. K.; Tekendo‐Ngongang, Cedrik; Fieggen, Karen; Prijoles, Eloise J.; Tanpaiboon, Pranoot; Honey, Engela; Luk, Ho‐Ming; Lo...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
1128
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗