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Search Results - Bartik, Lauren E.
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22q11.2 duplications: Expanding the clinical presentation
by
Bartik, Lauren E.
,
Hughes, Susan S.
,
Tracy, Meghan
,
Feldt, M. Max
,
Zhang, Lei
,
Arganbright, Jill
,
Kaye, Alison
Published in
American journal of medical genetics. Part A
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A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
by
Drivas, Theodore G
,
Li, Dong
,
Nair, Divya
,
Alaimo, Joseph T
,
Alders, Mariëlle
,
Altmüller, Janine
,
Barakat, Tahsin Stefan
,
Bebin, E Martina
,
Bertsch, Nicole L
,
Blackburn, Patrick R
,
Blesson, Alyssa
,
Bouman, Arjan M
,
Brockmann, Knut
,
Brunelle, Perrine
,
Burmeister, Margit
,
Cooper, Gregory M
,
Denecke, Jonas
,
Dieux-Coëslier, Anne
,
Dubbs, Holly
,
Ferrer, Alejandro
,
Gal, Danna
,
Bartik, Lauren E
,
Gunderson, Lauren B
,
Hasadsri, Linda
,
Jain, Mahim
,
Karimov, Catherine
,
Keena, Beth
,
Klee, Eric W
,
Kloth, Katja
,
Lace, Baiba
,
Macchiaiolo, Marina
,
Marcadier, Julien L
,
Milunsky, Jeff M
,
Napier, Melanie P
,
Ortiz-Gonzalez, Xilma R
,
Pichurin, Pavel N
,
Pinner, Jason
,
Powis, Zoe
,
Prasad, Chitra
,
Radio, Francesca Clementina
,
Rasmussen, Kristen J
,
Renaud, Deborah L
,
Rush, Eric T
,
Saunders, Carol
,
Selcen, Duygu
,
Seman, Ann R
,
Shinde, Deepali N
,
Smith, Erica D
,
Smol, Thomas
,
Snijders Blok, Lot
,
Stoler, Joan M
,
Tang, Sha
,
Tartaglia, Marco
,
Thompson, Michelle L
,
van de Kamp, Jiddeke M
,
Wang, Jingmin
,
Weise, Dagmar
,
Weiss, Karin
,
Woitschach, Rixa
,
Wollnik, Bernd
,
Yan, Huifang
,
Zackai, Elaine H
,
Zampino, Giuseppe
,
Campeau, Philippe
,
Bhoj, Elizabeth
Published in
European journal of human genetics : EJHG
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American Journal Of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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European Journal Of Human Genetics
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European Journal Of Human Genetics : Ejhg
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Abnormalities, Multiple - Diagnosis
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Adenosine Triphosphatase
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Chromosome 22Q11.2
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Chromosome Deletion
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Chromosome Duplication - Genetics
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Chromosome Microarray
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Chromosomes, Human, Pair 22 - Genetics
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