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Connection

Carmen Cadilla to Pedigree

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This is a "connection" page, showing publications Carmen Cadilla has written about Pedigree.
Carmen Cadilla
Connection Strength
0.297
Pedigree
  1. Serrano-Gonz?lez J, Montes-Rodr?guez I, Renta JY, Rojas R, Cadilla CL. After an initial Hermansky-Pudlak syndrome clinical diagnosis, molecular testing reveals variants for oculocutaneous albinism type 1B: A case report. Mol Genet Genomic Med. 2024 Jul; 12(7):e2493.
    View in: PubMed
    Score: 0.243
  2. Rosti RO, Uyguner ZO, Nazarenko I, Bekerecioglu M, Cadilla CL, Ozgur H, Lee BH, Aggarwal AK, Pehlivan S, Desnick RJ. Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation. Clin Genet. 2015 Nov; 88(5):489-493.
    View in: PubMed
    Score: 0.031
  3. Tukel T, ?o?ic D, Al-Gazali LI, Erazo M, Casasnovas J, Franco HL, Richardson JA, Olson EN, Cadilla CL, Desnick RJ. Homozygous nonsense mutations in TWIST2 cause Setleis syndrome. Am J Hum Genet. 2010 Aug 13; 87(2):289-96.
    View in: PubMed
    Score: 0.023
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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