Results
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3741.
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3742.
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3743.
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3744.
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3745.
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3749.
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3751.
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Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability. [electronic resource] by
- McBride, Kim L
- Pignatelli, Ricardo
- Lewin, Mark
- Ho, Trang
- Fernbach, Susan
- Menesses, Andres
- Lam, Wilbur
- Leal, Suzanne M
- Kaplan, Norman
- Schliekelman, Paul
- Towbin, Jeffrey A
- Belmont, John W
Producer: 20050627
In:
American journal of medical genetics. Part A vol. 134A
Availability: No items available.
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3752.
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3753.
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3754.
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Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF. [electronic resource] by
- Izumi, Kosuke
- Yahagi, Naohisa
- Fujii, Yasushi
- Higuchi, Masataka
- Kosaki, Rika
- Naito, Yoko
- Nishimura, Gen
- Hosokai, Noboru
- Takahashi, Takao
- Kosaki, Kenjiro
Producer: 20060323
In:
American journal of medical genetics. Part A vol. 140
Availability: No items available.
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3755.
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Should chromosome breakage studies be performed in patients with VACTERL association? [electronic resource] by
- Faivre, Laurence
- Portnoï, Marie France
- Pals, Gerard
- Stoppa-Lyonnet, Dominique
- Le Merrer, Martine
- Thauvin-Robinet, Christel
- Huet, Frédéric
- Mathew, Christopher G
- Joenje, Hans
- Verloes, Alain
- Baumann, Clarisse
Producer: 20050822
In:
American journal of medical genetics. Part A vol. 137
Availability: No items available.
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3756.
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3757.
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3758.
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3759.
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3760.
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Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome. [electronic resource] by
- Kang, S-H L
- Scheffer, A
- Ou, Z
- Li, J
- Scaglia, F
- Belmont, J
- Lalani, S R
- Roeder, E
- Enciso, V
- Braddock, S
- Buchholz, J
- Vacha, S
- Chinault, A C
- Cheung, S W
- Bacino, C A
Producer: 20071107
In:
Clinical genetics vol. 72
Availability: No items available.
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