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Lewanda, Amy Feldman
15
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1
De Novo Variant in the RPL27 Gene in a Second Infant with D..:
Glass, Joshua
;
Weston, Julia
;
Lewanda, Amy Feldman
..
Case Reports in Hematology. 2024 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1155/..
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2
Patterns of Dietary Supplement Use in Children with Down Sy..:
Lewanda, Amy Feldman
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Gallegos, Margo Faust
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Summar, Marshall
The Journal of Pediatrics. 201 (2018) - p. 100-105.e30 , 2018
Link:
https://doi.org/10.1016/..
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3
Intellectual disability and epilepsy due to the K/L‐mediate..:
Ward, David Isum
;
Buckley, Bethany A.
;
Leon, Eyby
...
American Journal of Medical Genetics Part A. 176 (2018) 3 - p. 551-559 , 2018
Link:
https://doi.org/10.1002/..
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4
Preoperative evaluation and comprehensive risk assessment f..:
Lewanda, Amy Feldman
;
Matisoff, Andrew
;
Revenis, Mary
...
Pediatric Anesthesia. 26 (2016) 4 - p. 356-362 , 2016
Link:
https://doi.org/10.1111/..
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5
Two craniosynostotic patients with 11q deletions, and revie..:
Lewanda, Amy Feldman
;
Morsey, Susan
;
Reid, Cheryl S.
.
American Journal of Medical Genetics. 59 (1995) 2 - p. 193-198 , 1995
Link:
https://doi.org/10.1002/..
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6
Genetic Heterogeneity among Craniosynostosis Syndromes: Map..:
Lewanda, Amy Feldman
;
Cohen Jr., M.Michael
;
Jackson, Charles E.
...
Genomics. 19 (1994) 1 - p. 115-119 , 1994
Link:
https://doi.org/10.1006/..
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7
Two Craniosynostotic Syndrome Loci, Crouzon and Jackson-Wei..:
Li, Xiang
;
Lewanda, Amy Feldman
;
Eluma, Fabian
...
Genomics. 22 (1994) 2 - p. 418-424 , 1994
Link:
https://doi.org/10.1006/..
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8
Genetics of craniofacial disorders:
Lewanda MD, Amy Feldman
;
Jabs, Ethylin Wang
Current Opinion in Pediatrics. 6 (1994) 6 - p. 690-697 , 1994
Link:
https://doi.org/10.1097/..
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9
Germline Saturation Mutagenesis Induces Skeletal Phenotypes..:
Rios, Jonathan J
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Denton, Kristin
;
Russell, Jamie
...
Journal of Bone and Mineral Research. 36 (2020) 8 - p. 1548-1565 , 2020
Link:
https://doi.org/10.1002/..
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10
No Evidence of Linkage for Cleft Lip with or without Cleft ..:
Wyszynski, Diego F.
;
Maestri, Nancy
;
Lewanda, Amy F.
...
Human Heredity. 47 (1997) 2 - p. 101-109 , 1997
Link:
https://www.jstor.org/st..
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11
No Evidence of Linkage for Cleft Lip with or without Cleft ..:
Wyszynski, Diego F.
;
Maestri, Nancy
;
Lewanda, Amy F.
...
Human Heredity. 47 (1997) 2 - p. 101-109 , 1997
Link:
https://doi.org/10.1159/..
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12
Evidence for an association between markers on chromosome 1..:
Wyszynski, D. F.
;
Maestri, Nancy
;
McIntosh, Iain
...
Human Genetics. 99 (1996) 1 - p. 22-26 , 1996
Link:
https://doi.org/10.1007/..
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13
P184: Hypermobility clinic: Innovative workflow supporting ..:
Chapman, Kimberly
;
Vause, Spencer
;
Berger, Seth
...
Genetics in Medicine Open. 2 (2024) - p. 101081 , 2024
Link:
https://doi.org/10.1016/..
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14
ATOH7 mutations cause autosomal recessive persistent hyperp..:
Prasov, Lev
;
Masud, Tehmina
;
Khaliq, Shagufta
...
Human Molecular Genetics. 21 (2012) 16 - p. 3681-3694 , 2012
Link:
https://doi.org/10.1093/..
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15
Clinical and molecular analysis of arylsulfatase E in patie..:
Nino, Michelle
;
Matos‐Miranda, Claudia
;
Maeda, Momoe
...
American Journal of Medical Genetics Part A. 146A (2008) 8 - p. 997-1008 , 2008
Link:
https://doi.org/10.1002/..
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