Search

Author/Creator Huckstadt, Victoria

1. Challenges in genetic diagnosis, co‐occurrence of 22q11.2 deletion syndrome and Noonan syndrome. Issue 8 (11th June 2022)

Authors:
Chinton, Josefina; Huckstadt, Victoria; Foncuberta, Maria Eugenia; Perez, Maria Mercedes; Bonetto, Mara Cecilia; Gravina, Luis Pablo; Obregon, María Gabriela
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 8(2022)
Page Start:
2505
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. 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
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Rubinstein–Taybi syndrome in diverse populations. Issue 12 (27th September 2020)

Authors:
Tekendo‐Ngongang, Cedrik; Owosela, Babajide; Fleischer, Nicole; Addissie, Yonit A.; Malonga, Bryan; Badoe, Ebenezer; Gupta, Neerja; Moresco, Angélica; Huckstadt, Victoria; Ashaat, Engy A.; Hussen, Dalia Farouk; Luk, Ho‐Ming; Lo, Ivan F. M.; Hon‐Yin Chung, Brian; Fung, Jasmine L. F.; Moretti‐Ferre...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 12(2020)
Page Start:
2939
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Turner syndrome in diverse populations. Issue 2 (19th December 2019)

Authors:
Kruszka, Paul; Addissie, Yonit A.; Tekendo‐Ngongang, Cedrik; Jones, Kelly L.; Savage, Sarah K.; Gupta, Neerja; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Paththinige, C. Sampath; Aravena, Teresa; Nampoothiri, Sheela; Yesodharan, Dhanya; Girisha, Katta M.; Patil, Siddaramappa Jagdish; Jamuar...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 2(2020)
Page Start:
303
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Variable pulmonary manifestations in Chitayat syndrome: Six additional affected individuals. Issue 9 (27th June 2020)

Authors:
Suter, Aude‐Annick; Santos‐Simarro, Fernando; Toerring, Pernille Mathiesen; Abad Perez, Angela; Ramos‐Mejia, Rosario; Heath, Karen E.; Huckstadt, Victoria; Parrón‐Pajares, Manuel; Mensah, Martin Atta; Hülsemann, Wiebke; Holtgrewe, Manuel; Mundlos, Stefan; Kornak, Uwe; Bartsch, Oliver; Ehmke, Nadja
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 9(2020)
Page Start:
2068
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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) ↗