J R Stelling

Summary

Country: USA

Publications

  1. ncbi Dominant transmission of imperforate hymen
    J R Stelling
    Department of Obstetrics, Gynecology, and Reproductive Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Massachusetts, Boston, USA
    Fertil Steril 74:1241-4. 2000
  2. ncbi Subcutaneous versus intramuscular administration of human chorionic gonadotropin during an in vitro fertilization cycle
    James R Stelling
    Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston IVF, Boston, Massachusetts, USA
    Fertil Steril 79:881-5. 2003
  3. ncbi Role for anti-Müllerian hormone in congenital absence of the uterus and vagina
    B L Resendes
    Department of Obstetrics and Gynecology, New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA
    Am J Med Genet 98:129-36. 2001

Collaborators

Detail Information

Publications3

  1. ncbi Dominant transmission of imperforate hymen
    J R Stelling
    Department of Obstetrics, Gynecology, and Reproductive Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Massachusetts, Boston, USA
    Fertil Steril 74:1241-4. 2000
    ..Imperforate hymen is an uncommon anomaly of the reproductive tract, occurring in approximately 0.1% of newborn females. The familial occurrence of imperforate hymen in a child, her mother, and her mother's monozygotic twin is reported...
  2. ncbi Subcutaneous versus intramuscular administration of human chorionic gonadotropin during an in vitro fertilization cycle
    James R Stelling
    Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston IVF, Boston, Massachusetts, USA
    Fertil Steril 79:881-5. 2003
    ..To confirm that hCG levels in follicular fluid and serum would be comparable between i.m. and s.c. administration of purified hCG...
  3. ncbi Role for anti-Müllerian hormone in congenital absence of the uterus and vagina
    B L Resendes
    Department of Obstetrics and Gynecology, New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA
    Am J Med Genet 98:129-36. 2001
    ..Because no mutations or rare DNA sequence polymorphisms were detected in the AMH and the AMHR genes in this group of CAUV patients, it is unlikely that either gene commonly has an etiologic role in CAUV...