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Author/Creator Moretti‐Ferreira, Danilo

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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4. 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
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5. Spread of X‐chromosome inactivation into autosomal regions in patients with unbalanced X‐autosome translocations and its phenotypic effects. Issue 8 (29th April 2021)

Authors:
Favilla, Bianca Pereira; Meloni, Vera Ayres; Perez, Ana Beatriz; Moretti‐Ferreira, Danilo; de Souza, Deise Helena; Bellucco, Fernanda Teixeira; Melaragno, Maria Isabel
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 8(2021)
Page Start:
2295
Record Type:
Journal Article
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6. 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
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7. X‐linked intellectual disability related genes disrupted by balanced X‐autosome translocations. Issue 8 (20th August 2015)

Authors:
Moysés‐Oliveira, Mariana; Guilherme, Roberta Santos; Meloni, Vera Ayres; Di Battista, Adriana; de Mello, Claudia Berlim; Bragagnolo, Silvia; Moretti‐Ferreira, Danilo; Kosyakova, Nadezda; Liehr, Thomas; Carvalheira, Gianna Maria; Melaragno, Maria Isabel
Journal:
American journal of medical genetics
Issue:
Volume 168:Issue 8(2015)
Page Start:
669
Record Type:
Journal Article
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