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Gambello, Michael J.
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1

P291: Where are all the kids with fragile X syndrome? A ret..:

Black, Paige ; Gambello, Michael ; Lichten, Lauren..
Genetics in Medicine Open.  2 (2024)  - p. 101187 , 2024
Link: https://doi.org/10.1016/..
 
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2

Musculoskeletal phenotypes in 3q29 deletion syndrome:

Pollak, Rebecca M. ; Tilmon, Jacob C. ; Murphy, Melissa M....
American Journal of Medical Genetics Part A.  191 (2023)  11 - p. 2749-2756 , 2023
Link: https://doi.org/10.1002/..
 
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3

Acute myeloid leukemia and dilated cardiomyopathy in a pedi..:

Murphey, Kristen ; George, Paul E. ; Pencheva, Bojana...
American Journal of Medical Genetics Part A.  188 (2022)  9 - p. 2707-2711 , 2022
Link: https://doi.org/10.1002/..
 
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4

Elevated homocysteine levels: What inborn errors of metabol..:

Gonzalez, Aixa ; Smith, Geoffrey Hughes ; Gambello, Michael J....
American Journal of Medical Genetics Part A.  191 (2022)  1 - p. 130-134 , 2022
Link: https://doi.org/10.1002/..
 
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5

Deep phenotyping in 3q29 deletion syndrome: recommendations..:

Sanchez Russo, Rossana ; Gambello, Michael J. ; Murphy, Melissa M....
Genetics in Medicine.  23 (2021)  5 - p. 872-880 , 2021
Link: https://doi.org/10.1038/..
 
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6

Case report of acute myeloid leukemia and dilated cardiomyo..:

Ferriero, Kristen ; George, Paul ; Pencheva, Bojana...
Molecular Genetics and Metabolism.  132 (2021)  - p. S18-S19 , 2021
Link: https://doi.org/10.1016/..
 
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7

Hypotrichosis‐lymphedema‐telangiectasia syndrome: Report of..:

Coulie, Richard ; Niyazov, Dmitriy M. ; Gambello, Michael J....
American Journal of Medical Genetics Part A.  185 (2021)  7 - p. 2153-2159 , 2021
Link: https://doi.org/10.1002/..
 
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8

Craniofacial features of 3q29 deletion syndrome: Applicatio..:

Mak, Bryan C. ; Sanchez Russo, Rossana ; Gambello, Michael J....
American Journal of Medical Genetics Part A.  185 (2021)  7 - p. 2094-2101 , 2021
Link: https://doi.org/10.1002/..
 
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9

Convergent and distributed effects of the 3q29 deletion on ..:

Sefik, Esra ; Purcell, Ryan H. ; Aberizk, Katrina...
Translational Psychiatry.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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10

Correction: The CHD4-related syndrome: a comprehensive inve..:

Weiss, Karin ; Lazar, Hayley P. ; Kurolap, Alina...
Genetics in Medicine.  22 (2020)  3 - p. 669 , 2020
Link: https://doi.org/10.1038/..
 
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11

Increased parental anxiety and a benign clinical course: In..:

Sadat, Roa ; Hall, Patricia L. ; Wittenauer, Angela L....
Molecular Genetics and Metabolism.  129 (2020)  1 - p. 20-25 , 2020
Link: https://doi.org/10.1016/..
 
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12

Ornithine decarboxylase, the rate-limiting enzyme of polyam..:

Kapfhamer, David ; McKenna III, James ; Yoon, Caroline J...
Human Molecular Genetics.  29 (2020)  14 - p. 2395-2407 , 2020
Link: https://doi.org/10.1093/..
 
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13

The CHD4-related syndrome: a comprehensive investigation of..:

Weiss, Karin ; Lazar, Hayley P. ; Kurolap, Alina...
Genetics in Medicine.  22 (2020)  2 - p. 389-397 , 2020
Link: https://doi.org/10.1038/..
 
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14

Comprehensive phenotyping of neuropsychiatric traits in a m..:

The Emory 3q29 Project ; Murphy, Melissa M. ; Burrell, T. Lindsey...
BMC Psychiatry.  20 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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15

Primrose syndrome: Characterization of the phenotype in 42 ..:

Melis, Daniela ; Carvalho, Daniel ; Barbaro‐Dieber, Tina...
Clinical Genetics.  97 (2020)  6 - p. 890-901 , 2020
Link: https://doi.org/10.1111/..
 
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