Search Results - "Ulm, J E"

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  1. 1
    Prenatal diagnosis of sickle cell anemia. Hemoglobin electrophoresis versus DNA analysis

    Prenatal diagnosis of sickle cell anemia. Hemoglobin electrophoresis versus DNA analysis by Posey, Y F, Shah, D, Ulm, J E, Bastin, K T, Parl, F F, Phillips, 3rd, J A

    Published in American journal of clinical pathology (01-09-1989)
    “…The prenatal diagnosis of sickle cell anemia (hemoglobin SS) can be established by DNA analysis using two highly sensitive techniques (Southern blot and…”
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  2. 2
    Diagnosis of trisomy 18 in monozygotic twins by cordocentesis

    Diagnosis of trisomy 18 in monozygotic twins by cordocentesis by Shah, D M, Jeanty, P, Dev, V G, Ulm, J E, Phillips, J

    “…The incidence of monozygotic twins with trisomy 18 is 1 in 1,000,000 births. We report a case diagnosed prenatally with lymphocyte culture from fetal blood…”
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  3. 3
    Counseling and decision dilemmas associated with fetal blood sampling

    Counseling and decision dilemmas associated with fetal blood sampling by Ulm, J E, Shah, D M, Dev, V G, Phillips, 3rd, J A

    Published in American journal of medical genetics (01-01-1990)
    “…Counseling before fetal blood sampling via cordocentesis is more difficult than that done before amniocentesis because 1) a fetal anomaly has been detected or…”
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  4. 4
    The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis

    The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis by Butler, M G, Dev, V G, Shah, D, Ulm, J E, Wilmot, P L, Shapiro, L R

    Published in American journal of medical genetics (01-12-1988)
    “…Early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal diagnosis were undertaken for the first time in a 17-week…”
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  5. 5
    Prenatal diagnosis of a der(X)t(X;15)(p22.2;q11.2) inherited from a maternal translocation X;15

    Prenatal diagnosis of a der(X)t(X;15)(p22.2;q11.2) inherited from a maternal translocation X;15 by Garcia-Heras, Jaime, Ulm, Janet E., Shaver, David E., Hall, Eric, Saikevych, Irene A.

    Published in Prenatal diagnosis (01-07-1998)
    “…A karyotype 46,X,der(X)t(X;15)(p22.2;q11.2) derived from a maternal translocation X;15 was ascertained in a female fetus through an abnormal triple screen test…”
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  6. 6
    Newborn screening for galactosemia in Tennessee

    Newborn screening for galactosemia in Tennessee by Ulm, J E

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  7. 7
    Recurrent Trisomies: Chance or Inherited Predisposition?

    Recurrent Trisomies: Chance or Inherited Predisposition? by Ulm, Janet E.

    Published in Journal of genetic counseling (01-04-1999)
    “…Two patients experiencing recurring trisomic pregnancies involving a different chromosome each time are presented. Mechanisms to explain recurrent trisomies…”
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  8. 8
    Prenatal diagnosis of a der(X)t(X;15)p22.2;q11.2 inherited from a maternal translocation x;15

    Prenatal diagnosis of a der(X)t(X;15)p22.2;q11.2 inherited from a maternal translocation x;15 by GARCIA-HERAS, J, ULM, J. E, SHAVER, D. E, HALL, E, SAIKEVYCH, I. A

    Published in Prenatal diagnosis (1998)
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