Results 1 -
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19
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Fetal anomaly
- 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 ...
- ... M. Congenital alveolar capillary dysplasia and associated gastrointestinal anomalies. Fetal Pediatr Pathol. 2006 May-Jun;25(3):137- ...
- ... Noort G, Waterham HR, Hall CM, Hennekam RC. Congenital abnormalities reported in Pelger-Huet homozygosity as compared to ...
- ... of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of ...
- ... 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 ...
- ... reproductive cells (eggs or sperm) or in early fetal development. Affected people ... syndrome Conotruncal anomaly face syndrome (CTAF) Deletion 22q11.2 syndrome DiGeorge ...
- ... 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 ...
- ... reproductive cells (eggs or sperm) or in early fetal development. Affected people typically ... anomalies, and mental retardation syndrome Wilms tumor-aniridia-genital ...
- ... review of 78 cases diagnosed by prenatal sonography. Fetal Diagn Ther. 2004 ... anomalies, incidence of hydrocephalus, and developmental outcomes. J Neurosurg ...
- ... 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( ...