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Results 1 - 10 of 19 for Fetal anomaly
  1. 17q12 deletion syndrome is a condition that results from the deletion of a small piece of chromosome 17 in each cell. The deletion occurs on the long (q) arm ...
  2. ... M. Congenital alveolar capillary dysplasia and associated gastrointestinal anomalies. Fetal Pediatr Pathol. 2006 May-Jun;25(3):137- ...
  3. ... Noort G, Waterham HR, Hall CM, Hennekam RC. Congenital abnormalities reported in Pelger-Huet homozygosity as compared to ...
  4. ... of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of ...
  5. ... reproductive cells (eggs and sperm) or in early fetal development. They may also result from a new mutation in the HCCS ... Microphthalmia with linear skin defects syndrome National ...
  6. ... reproductive cells (eggs or sperm) or in early fetal development. Affected people ... syndrome Conotruncal anomaly face syndrome (CTAF) Deletion 22q11.2 syndrome DiGeorge ...
  7. ... as a major gene in Rokitansky-Kuster-Hauser anomaly. Am J Med Genet A. 2005 Aug ... expressed in human fetal and adult ovaries and its signaling contributes to ...
  8. ... reproductive cells (eggs or sperm) or in early fetal development. Affected people typically ... anomalies, and mental retardation syndrome Wilms tumor-aniridia-genital ...
  9. ... review of 78 cases diagnosed by prenatal sonography. Fetal Diagn Ther. 2004 ... anomalies, incidence of hydrocephalus, and developmental outcomes. J Neurosurg ...
  10. ... an affected individual's parent or in early fetal development. These cases occur in people with no history of the disorder ... deletions: delineating the critical region for urogenital anomalies. Am J Med Genet A. 2015 Apr;167A( ...
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