Search Results - Jaloma-Cruz, Ana R

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q

    Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q by Vásquez-Velásquez, Ana I, Rivera, Horacio, Castro, Ana G, Jaloma-Cruz, Ana R, Juárez, Clara I, Lara-Navarro, Irving J, Córdova-Fletes, Carlos, Mendoza- Pérez, Paul, García-Ortiz, José E

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans

    Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans by Drost, Joni B., Scaringe, William A., Jaloma-Cruz, Ana Rebeca, Li, Xuemin, Ossa, Diego F., Kasper, Carol K., Sommer, Steve S.

    Published in Human mutation
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  3. 3
    Y-Chromosome Haplotypes for Six Short Tandem Repeats (STRs) in a Mexican Population

    Y-Chromosome Haplotypes for Six Short Tandem Repeats (STRs) in a Mexican Population by Rangel-Villalobos, Héctor, Jaloma-Cruz, Ana Rebeca, Sandoval-Ramı́rez, Lucila, Velarde-Félix, Jesús Salvador, Gallegos-Arreola, Martha Patricia, Figuera, Luis Eduardo

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Nine independent F9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline

    Nine independent F9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline by Jaloma-Cruz, Ana Rebeca, Scaringe, William A., Drost, Joni B., Roberts, Stacy, Li, Xuemin, Barros-Núñez, Patricio, Figuera, Luis E., Rivas, Fernando, Cantú, José María, Sommer, Steve S.

    Published in Human mutation
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: