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Hufnagel RB 8

Showing records 1 to 8 | Display all abstracts from Hufnagel RB

99231 Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
Ahmed MR
Genes 2022; 13:

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98018
Prasov L; Prasov L; Bohnsack BL
Journal of Medical Genetics 2022; 59: 294-304

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99231 Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
Sethna S; Krueger LA
Genes 2022; 13:

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98018
El Husny AS; Tsoi LC
Journal of Medical Genetics 2022; 59: 294-304

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99231 Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
Yang MB; Hufnagel RB
Genes 2022; 13:

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98018
Guan B
Journal of Medical Genetics 2022; 59: 294-304

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99231 Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
Hufnagel RB
Genes 2022; 13:

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98018
Kahlenberg JM; Almeida E; Wang H; Cowen EW; De Jesus AA; Jani P; Billi AC; Moroi SE; Wasikowski R; Almeida I; Almeida LN; Kok F; Garnai SJ; Mian SI; Chen MY; Warner BM; Ferreira CR; Goldbach-Mansky R; Hur S; Brooks BP; Richards JE; Hufnagel RB; Hufnagel RB; Gudjonsson JE
Journal of Medical Genetics 2022; 59: 294-304

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