Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lillian L Lockhart"'
Publikováno v:
British Journal of Haematology. 107:49-54
Pregnancy in bone marrow failure syndromes has risk to mother and fetus. There are fewer than 30 reports of cases with Diamond-Blackfan anaemia (DBA), and none with Shwachman-Diamond syndrome (SD). We report two DBA and one SD cases. One DBA mother r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454f500350ed5374c76b74117cd6a95d
https://doi.org/10.1046/j.1365-2141.1999.01668.x
https://doi.org/10.1046/j.1365-2141.1999.01668.x
Autor:
Lillian L Lockhart, Jill K. Northup, Kathleen Griffis, Gopalrao V.N. Velagaleti, Judy C. Hawkins
Publikováno v:
Fertility and sterility. 87(3)
Objective To provide a hypothesis regarding the cause of premature ovarian failure (POF) observed in a 27-year-old with a mosaic dicentric chromosome. Design Case report. Setting Cytogenetics/molecular cytogenetics laboratory in a university hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b5424cbaeab32ee4a4f4ec5cc5fa8e5
https://pubmed.ncbi.nlm.nih.gov/17140574
https://pubmed.ncbi.nlm.nih.gov/17140574
Publikováno v:
Human Genetics. 67:233-236
An interstitial deletion of the long arm of chromosome 16 has been identified in identical twins. These patients are strikingly similar phenotypically to previously reported cases of deletion 16q syndrome but differ chromosomally in that their deleti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2757bb58dc3448d7a00e28abf8e0bc48
https://doi.org/10.1007/bf00273010
https://doi.org/10.1007/bf00273010
Congenital idiopathic hypertrophic subaortic stenosis associated with a phenotypic Turner's syndrome
Autor:
Jose R. Toledo, Lillian L Lockhart, Melvyn H. Schreiber, Quang X. Nghiem, Kenneth R.T. Tyson, Leonard C. Harris
Publikováno v:
The American Journal of Cardiology. 30:683-689
A case of idiopathic hypertrophic subaortic stenosis in a girl with phenotypic Turner's syndrome is reported. The coincidence of these rare anomalies, reported only once before, is unlikely to occur by chance. Essential clinical features leading to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97918af5939c28d39fa4c7dcd157b957
https://doi.org/10.1016/0002-9149(72)90611-x
https://doi.org/10.1016/0002-9149(72)90611-x
Publikováno v:
Pediatric Research. 12:416-416
The etiology of the genital anomalies in two unrelated teenagers with male pseudohermaphroditism and renal disease has been investigated. Patient A, 15-5/12 year old XY black, has stage 5 pubic hair, perineal hypospadius, 3 cc firm descended right te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd1972f0d15508a1f3f33f716d4cc09b
https://doi.org/10.1203/00006450-197804001-00319
https://doi.org/10.1203/00006450-197804001-00319
Autor:
Northup J; Department of Pathology, University of Texas Medical Branch, Galveston, Texas 77555-0359, USA., Griffis K, Hawkins J, Lockhart L, Velagaleti G
Publikováno v:
Fertility and sterility [Fertil Steril] 2007 Mar; Vol. 87 (3), pp. 697.e5-8. Date of Electronic Publication: 2006 Nov 29.