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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 18, 2018
Syndromes associated with holoprosencephalyPaul Kruszka, Maximilian Muenke
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 18, 2018
Molecular testing in holoprosencephalyPaul Kruszka, Ariel F Martinez, Maximilian Muenke
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 6, 2018
Challenging issues arising in counseling families experiencing holoprosencephalyDonald W Hadley, Paul Kruszka, Maximilian Muenke
Current Opinion in Pediatrics|November 7, 2019
Diversity and dysmorphologyPaul Kruszka, Cedrik Tekendo-Ngongang, Maximilian Muenke
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 6, 2020
Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specificCedrik Tekendo-Ngongang, Babajide Owosela, Maximilian Muenke, et al.
Clinical Genetics|July 9, 2019
Novel heterozygous variants in KMT2D associated with holoprosencephalyCedrik Tekendo-Ngongang, Paul Kruszka, Ariel F Martinez, et al.
American Journal of Medical Genetics. Part A|October 27, 2022
Hajdu-Cheney syndrome with atypical cardiovascular abnormalitiesEkanem N Ekure, Ogochukwu Sokunbi, Paul Kruszka, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 11, 2018
Low-level parental mosaicism affects the recurrence risk of holoprosencephalyPing Hu, Ariel F Martinez, Paul Kruszka, et al.
Anatomical Record (Hoboken, N.J. : 2007)|April 18, 2018
Clinical and Demographic Evaluation of a Holoprosencephaly Cohort From the Kyoto Collection of Human EmbryosYu Abe, Paul Kruszka, Ariel F Martinez, et al.
American Journal of Medical Genetics. Part A|June 14, 2023
Ambiguous genitalia, giant congenital melanocytic nevus and subpulmonic outlet ventricular septal defect in an African child with Neurofibromatosis 1Ekanem N Ekure, Kareem O Musa, Ngozi Ulonnam, et al.
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