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Deletion of chromosome 8q22.1, a critical region for Nablus mask-like facial syndrome: four additional cases support a role of genetic modifiers in the manifestation of the phenotype. [electronic resource] by
- Jamuar, Saumya S
- Duzkale, Hatice
- Duzkale, Neslihan
- Zhang, Chengsheng
- High, Frances A
- Kaban, Leonard
- Bhattacharya, Soma
- Crandall, Barbara
- Kantarci, Sibel
- Stoler, Joan M
- Lin, Angela E
Producer: 20160217
In:
American journal of medical genetics. Part A vol. 167
Availability: No items available.
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70.
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71.
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Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance. [electronic resource] by
- Jones, Kelly L
- McNamara, Erin A
- Longoni, Mauro
- Miller, Danny E
- Rohanizadegan, Mersedeh
- Newman, Laura A
- Hayes, Frances
- Levitsky, Lynne L
- Herrington, Betty L
- Lin, Angela E
Producer: 20190925
In:
American journal of medical genetics. Part A vol. 176
Availability: No items available.
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72.
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Adults with Sotos syndrome: review of 21 adults with molecularly confirmed NSD1 alterations, including a detailed case report of the oldest person. [electronic resource] by
- Fickie, Matthew R
- Lapunzina, Pablo
- Gentile, Jennifer K
- Tolkoff-Rubin, Nina
- Kroshinsky, Daniela
- Galan, Enrique
- Gean, Esther
- Martorell, Loreto
- Romanelli, Valeria
- Toral, Joaquín Fernandez
- Lin, Angela E
Producer: 20120209
In:
American journal of medical genetics. Part A vol. 155A
Availability: No items available.
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73.
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An application of data mining to identify potential risk factors for anophthalmia and microphthalmia. [electronic resource] by
- Weber, Kari A
- Yang, Wei
- Carmichael, Suzan L
- Lupo, Philip J
- Dukhovny, Stephanie
- Yazdy, Mahsa M
- Lin, Angela E
- Van Bennekom, Carla M
- Mitchell, Allen A
- Shaw, Gary M
Producer: 20190307
In:
Paediatric and perinatal epidemiology vol. 32
Availability: No items available.
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74.
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Twinning and major birth defects, National Birth Defects Prevention Study, 1997-2007. [electronic resource] by
- Dawson, April L
- Tinker, Sarah C
- Jamieson, Denise J
- Hobbs, Charlotte A
- Berry, R J
- Rasmussen, Sonja A
- Anderka, Marlene
- Keppler-Noreuil, Kim M
- Lin, Angela E
- Reefhuis, Jennita
Producer: 20180108
In:
Journal of epidemiology and community health vol. 70
Availability: No items available.
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75.
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TFAP2A mutations result in branchio-oculo-facial syndrome. [electronic resource] by
- Milunsky, Jeff M
- Maher, Tom A
- Zhao, Geping
- Roberts, Amy E
- Stalker, Heather J
- Zori, Roberto T
- Burch, Michelle N
- Clemens, Michele
- Mulliken, John B
- Smith, Rosemarie
- Lin, Angela E
Producer: 20080716
In:
American journal of human genetics vol. 82
Availability: No items available.
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76.
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Maternal thyroid disease, thyroid medication use, and selected birth defects in the National Birth Defects Prevention Study. [electronic resource] by
- Browne, Marilyn L
- Rasmussen, Sonja A
- Hoyt, Adrienne T
- Waller, D Kim
- Druschel, Charlotte M
- Caton, Alissa R
- Canfield, Mark A
- Lin, Angela E
- Carmichael, Suzan L
- Romitti, Paul A
Producer: 20091022
In:
Birth defects research. Part A, Clinical and molecular teratology vol. 85
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77.
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Antihypertensive medication use during pregnancy and the risk of cardiovascular malformations. [electronic resource] by
- Caton, Alissa R
- Bell, Erin M
- Druschel, Charlotte M
- Werler, Martha M
- Lin, Angela E
- Browne, Marilyn L
- McNutt, Louise-Anne
- Romitti, Paul A
- Mitchell, Allen A
- Olney, Richard S
- Correa, Adolfo
Producer: 20090916
In:
Hypertension (Dallas, Tex. : 1979) vol. 54
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78.
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Further delineation of cardiac abnormalities in Costello syndrome. [electronic resource] by
- Lin, Angela E
- Grossfeld, Paul D
- Hamilton, Robert M
- Smoot, Leslie
- Gripp, Karen W
- Proud, Virginia
- Weksberg, Rosanna
- Wheeler, Patricia
- Picker, Jonathan
- Irons, Mira
- Zackai, Elaine
- Marino, Bradley
- Scott, Charles I
- Nicholson, Linda
Producer: 20030131
In:
American journal of medical genetics vol. 111
Availability: No items available.
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79.
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Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia. [electronic resource] by
- Lin, Angela E
- O'Brien, Barbara
- Demmer, Laurie A
- Almeda, Kristina K
- Blanco, Cynthia L
- Glasow, Patrick F
- Berul, Charles I
- Hamilton, Robert
- Micheil Innes, A
- Lauzon, Julie L
- Sol-Church, Katia
- Gripp, Karen W
Producer: 20091002
In:
Prenatal diagnosis vol. 29
Availability: No items available.
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80.
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Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. [electronic resource] by
- Prakash, Siddharth K
- Bondy, Carolyn A
- Maslen, Cheryl L
- Silberbach, Michael
- Lin, Angela E
- Perrone, Laura
- Limongelli, Giuseppe
- Michelena, Hector I
- Bossone, Eduardo
- Citro, Rodolfo
- Lemaire, Scott A
- Body, Simon C
- Milewicz, Dianna M
Producer: 20171016
In:
American journal of medical genetics. Part A vol. 170
Availability: No items available.
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