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Results 1 - 10 of 52 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. FMR1 gene 
    ... or Free article on PubMed Central Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB Jr, Moine ... Navarro CS, Tassone F, Kros JM, Severijnen LA, Berry-Kravis EM, Berman RF, Hagerman PJ, Willemsen R, ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  3. 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
  4. PHOX2B gene 
    ... PAIRED-LIKE HOMEOBOX 2B; PHOX2B NCBI Gene ClinVar Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer ... Repetto GM, Corrales RJ, Abara SG, Zhou L, Berry-Kravis EM, Rand CM, Weese-Mayer DE. Later- ...
    https://medlineplus.gov/genetics/gene/phox2b - Genetics
  5. 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
  6. PITX2 gene 
    ... RING DERMOID OF CORNEA; RDC NCBI Gene ClinVar Berry FB, Lines MA, Oas JM, Footz T, Underhill ... on PubMed Strungaru MH, Footz T, Liu Y, Berry FB, Belleau P, Semina EV, Raymond V, Walter ...
    https://medlineplus.gov/genetics/gene/pitx2 - Genetics
  7. 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
  8. 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
  9. 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
  10. OXCT1 gene 
    ... OXOACID CoA TRANSFERASE 1; OXCT1 NCBI Gene ClinVar 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/genetics/gene/oxct1 - Genetics
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