Common mutation causes cystinosis in the majority of black South African patients. Pediatric nephrology (Berlin, Germany) 2015 Apr 30 (4): 595-601. Owen E Patricia, Nandhlal Jenisha, Leisegang Felicity, Van der Watt George, Nourse Peter, Gajjar Pri |
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes. American journal of obstetrics and gynecology 2015 Mar 212 (3): 332.e1-9. Wapner Ronald J, Babiarz Joshua E, Levy Brynn, Stosic Melissa, Zimmermann Bernhard, Sigurjonsson Styrmir, Wayham Nicholas, Ryan Allison, Banjevic Milena, Lacroute Phil, Hu Jing, Hall Megan P, Demko Zachary, Siddiqui Asim, Rabinowitz Matthew, Gross Susan J, Hill Matthew, Benn Pet |
The First Case Report in Italy of Di George Syndrome Detected by Noninvasive Prenatal Testing. Case reports in obstetrics and gynecology 2015 2015 813104. Rapacchia Giuseppina, Lapucci Cristina, Pittalis Maria Carla, Youssef Aly, Farina Anton |
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients. American journal of medical genetics. Part C, Seminars in medical genetics 2013 Nov 163C (4): 259-70. Roscioli T, Elakis G, Cox T C, Moon D J, Venselaar H, Turner A M, Le T, Hackett E, Haan E, Colley A, Mowat D, Worgan L, Kirk E P, Sachdev R, Thompson E, Gabbett M, McGaughran J, Gibson K, Gattas M, Freckmann M-L, Dixon J, Hoefsloot L, Field M, Hackett A, Kamien B, Edwards M, Adès L C, Collins F A, Wilson M J, Savarirayan R, Tan T Y, Amor D J, McGillivray G, White S M, Glass I A, David D J, Anderson P J, Gianoutsos M, Buckley M |
Attitudes and beliefs of African-Americans toward genetics, genetic testing, and sickle cell disease education and awareness. Journal of genetic counseling 2011 Dec 20 (6): 572-92. Long Katie A, Thomas Stephen B, Grubs Robin E, Gettig Elizabeth A, Krishnamurti Lakshman |
Workforce and Patient Safety. April 24, 2024
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