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Author/Creator Sanchez‐Lara, Pedro A.

1. A celebration in honor of John M. Graham, Jr, MD, ScD. Issue 9 (10th July 2021)

Authors:
D'Cunha Burkardt, Deepika; Sanchez‐Lara, Pedro A.; Girisha, Katta M.; Golden, Jeffrey A.; Carey, John C.
Other Names:
Burkardt Deepika D'Cunha guestEditor.; Sanchez‐Lara Pedro A guestEditor.; Girisha Katta M guestEditor.; Carey John C guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 9(2021)
Page Start:
2617
Record Type:
Journal Article
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2. Characterization of sleep habits of children with Sotos syndrome. Issue 9 (24th April 2021)

Authors:
Stafford, Christine F.; Ward, Carrie; Ward, Sally L. D.; Sanchez‐Lara, Pedro A.
Other Names:
Burkardt Deepika D'Cunha guestEditor.; Sanchez‐Lara Pedro A guestEditor.; Girisha Katta M guestEditor.; Carey John C guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 9(2021)
Page Start:
2815
Record Type:
Journal Article
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3. Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome. Issue 6 (30th March 2021)

Authors:
Sheppard, Sarah E.; Campbell, Ian M.; Harr, Margaret H.; Gold, Nina; Li, Dong; Bjornsson, Hans T.; Cohen, Julie S.; Fahrner, Jill A.; Fatemi, Ali; Harris, Jacqueline R.; Nowak, Catherine; Stevens, Cathy A.; Grand, Katheryn; Au, Margaret; Graham, John M.; Sanchez‐Lara, Pedro A.; Campo, Miguel Del;...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 6(2021)
Page Start:
1649
Record Type:
Journal Article
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4. Expanding the phenotypic spectrum of RPL13‐related skeletal dysplasia. Issue 9 (27th November 2020)

Authors:
Reinsch, Breann; Grand, Katheryn; Lachman, Ralph S.; Kim, Harry K. W.; Sanchez‐Lara, Pedro A.
Other Names:
Burkardt Deepika D'Cunha guestEditor.; Sanchez‐Lara Pedro A guestEditor.; Girisha Katta M guestEditor.; Carey John C guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 9(2021)
Page Start:
2776
Record Type:
Journal Article
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5. Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. Issue 7 (30th March 2021)

Authors:
Hildebrandt, Clara C.; Patel, Nisha; Graham, John M.; Bamshad, Michael; Nickerson, Deborah A.; White, Janson J.; Marvin, Colby T.; Miller, Danny E.; Grand, Katheryn L.; Sanchez‐Lara, Pedro A.; Schweitzer, Daniela; Al‐Zaidan, Hamad I.; Al Masseri, Zainab; Alkuraya, Fowzan S.; Lin, Angela E.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 7(2021)
Page Start:
2136
Record Type:
Journal Article
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7. Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians1. Issue 10 (5th August 2014)

Authors:
Figueiredo, Jane C.; Ly, Stephanie; Raimondi, Haley; Magee, Kathy; Baurley, James W.; Sanchez‐Lara, Pedro A.; Ihenacho, Ugonna; Yao, Caroline; Edlund, Christopher K.; van den Berg, David; Casey, Graham; DeClerk, Yves A.; Samet, Jonathan M.; Magee, William
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 10(2014.)
Page Start:
2572
Record Type:
Journal Article
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8. Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians1. Issue 10 (5th August 2014)

Authors:
Figueiredo, Jane C.; Ly, Stephanie; Raimondi, Haley; Magee, Kathy; Baurley, James W.; Sanchez‐Lara, Pedro A.; Ihenacho, Ugonna; Yao, Caroline; Edlund, Christopher K.; van den Berg, David; Casey, Graham; DeClerk, Yves A.; Samet, Jonathan M.; Magee, William
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 10(2014.)
Page Start:
2572
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects. Issue 7 (6th April 2022)

Authors:
Munabi, Naikhoba C. O.; Mikhail, Shady; Toubat, Omar; Webb, Michelle; Auslander, Allyn; Sanchez‐Lara, Pedro A.; Manojlovic, Zarko; Schmidt, Ryan J.; Craig, David; Magee, William P.; Kumar, Subramanyan Ram
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 7(2022)
Page Start:
2082
Record Type:
Journal Article
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10. Hypoxia: A teratogen underlying a range of congenital disruptions, dysplasias, and malformations. Issue 9 (3rd May 2021)

Authors:
Adam, Aaron P.; Payton, Kurlen S. E.; Sanchez‐Lara, Pedro A.; Adam, Margaret P.; Mirzaa, Ghayda M.
Other Names:
Burkardt Deepika D'Cunha guestEditor.; Sanchez‐Lara Pedro A guestEditor.; Girisha Katta M guestEditor.; Carey John C guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 9(2021)
Page Start:
2801
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗