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Results 1 - 10 of 29 for Berries
  1. Congenital central hypoventilation syndrome 
    ... Turkington P, Windisch W, Samuels M, Stevens CA, Berry-Kravis EM, Weese-Mayer DE. PHOX2B mutation-confirmed ... 607CR. Epub 2006 Jul 27. Citation on PubMed Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
  2. Hereditary fructose intolerance 
    ... Fructose is a simple sugar found primarily in fruits. Affected individuals develop signs and symptoms of the disorder in infancy when fruits, juices, or other foods containing fructose are introduced ...
    https://medlineplus.gov/.../hereditary-fructose-intolerance - Genetics
  3. Galactosemia 
    ... GALAC2 GALACTOSEMIA III; GALAC3 GALACTOSEMIA I; GALAC1 PubMed Berry GT. Classic Galactosemia and Clinical Variant Galactosemia. 2000 ... nlm.nih.gov/books/NBK1518/ Citation on PubMed Berry GT. Galactosemia: when is it a newborn screening ...
    https://medlineplus.gov/genetics/condition/galactosemia - Genetics
  4. Succinyl-CoA:3-ketoacid CoA transferase deficiency 
    ... CoA:3-OXOACID-CoA TRANSFERASE DEFICIENCY; SCOTD PubMed Berry GT, Fukao T, Mitchell GA, Mazur A, Ciafre ... JE, Besley G, Wanders RJ, Niezen-Koning KE, Berry GT, Palmieri M, Kondo N. Succinyl-CoA:3- ...
    https://medlineplus.gov/...-coa3-ketoacid-coa-transferase-deficiency - Genetics
  5. Congenital sucrase-isomaltase deficiency 
    ... sucrose and maltose. Sucrose (a sugar found in fruits, and also known as table sugar) and maltose ( ... an infant is weaned and starts to consume fruits, juices, grains, and other starchy food. After ingestion ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  6. Fragile X syndrome 
    ... 1-00297.x. Citation on PubMed Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB Jr, Moine ... nrdp.2017.65. Citation on PubMed Hunter JE, Berry-Kravis E, Hipp H, Todd PK. FMR1 Disorders. ...
    https://medlineplus.gov/genetics/condition/fragile-x-syndrome - Genetics
  7. 15q13.3 microdeletion 
    ... Citation on PubMed Ziats MN, Goin-Kochel RP, Berry LN, Ali M, Ge J, Guffey D, Rosenfeld ...
    https://medlineplus.gov/genetics/condition/15q133-microdeletion - Genetics
  8. Congenital contractural arachnodactyly 
    ... Steinmann B, Child A, Danesino C, Metcalfe K, Berry SA, Chen E, Delorme CV, Thong MK, Ades ...
    https://medlineplus.gov/.../congenital-contractural-arachnodactyly - Genetics
  9. Propionic acidemia 
    ... gov PROPIONIC ACIDEMIA PubMed Aldubayan SH, Rodan LH, Berry GT, Levy HL. Acute Illness Protocol for Organic ...
    https://medlineplus.gov/genetics/condition/propionic-acidemia - Genetics
  10. Fragile X-associated primary ovarian insufficiency 
    ... 2007 Jun 22. Citation on PubMed Hunter JE, Berry-Kravis E, Hipp H, Todd PK. FMR1 Disorders. ...
    https://medlineplus.gov/...-associated-primary-ovarian-insufficiency - Genetics
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