Found: 7
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Mosaic Duplication 1(q11q44) in an Infant With Nephroblastomatosis and Mineralization of Extraplacental Membranes.
- Published in:
- Pediatric & Developmental Pathology, 2005, v. 8, n. 1, p. 115, doi. 10.1007/s10024-003-9098-4
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- Publication type:
- Article
Incidental detection of premature centromere separation in amniocytes associated with a mild form of Roberts syndrome.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 8, p. 565, doi. 10.1002/pd.1970080803
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- Publication type:
- Article
Developmental Delay: Timely Identification and Assessment.
- Published in:
- Indian Pediatrics, 2010, v. 47, n. 5, p. 415, doi. 10.1007/s13312-010-0077-3
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- Publication type:
- Article
[<sup>13</sup>C]‐galactose breath test in a patient with galactokinase deficiency and spastic diparesis.
- Published in:
- Journal of Inherited Metabolic Disease Reports, 2021, v. 59, n. 1, p. 104, doi. 10.1002/jmd2.12205
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- Publication type:
- Article
Neurologic Disease in a Child With Hepatoerythropoietic Porphyria.
- Published in:
- Pediatric Dermatology, 1994, v. 11, n. 3, p. 216, doi. 10.1111/j.1525-1470.1994.tb00589.x
- By:
- Publication type:
- Article
Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome.
- Published in:
- Annals of Neurology, 1992, v. 32, n. 4, p. 512, doi. 10.1002/ana.410320406
- By:
- Publication type:
- Article
Genetic counseling in pediatric practice.
- Published in:
- 1986
- By:
- Publication type:
- journal article