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11. Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita. Issue 6 (5th April 2021)

13. RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. Issue 7 (13th April 2011)

14. Severe X‐linked chondrodysplasia punctata in nine new female fetuses. (30th March 2015)

16. Variable prenatal presentation of Pfeiffer syndrome: Suggested aids to prenatal sonographic diagnosis. (28th February 2018)