Physician
Medical Genetics
Dr. Susan R. Panny, MD
Susan Panny practices Medical Genetics. She went to medical school at University of Maryland School of Medicine. University of Maryland School of Medicine is ranked 37/52 in Research/PrimaryCare. Susan R. Panny, MD is a published doctor. She published 29 publications, including: 'Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency.'
Publications
- Newborn screening for X-linked adrenoleukodystrophy: Further evidence high throughput screening is feasible.
- False negative cystic fibrosis newborn screen.
- Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) method.
- Birth delivery mode modifies the associations between prenatal polychlorinated biphenyl (PCB) and polybrominated diphenyl ether (PBDE) and neonatal thyroid hormone lev...
- Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies.
- Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996.
- Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency.
- US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Serv...
- A case-control study of nonsyndromic oral clefts in Maryland.
- Characteristics influencing informed consent on a congenital malformations registry.
- Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.
- Epidemiology of sentinel birth defects in Maryland, 1984.
- A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.
- A temperature sensitive mutation of the beta''-subunit of DNA-dependent RNA polymerase from E. coli T 16.
- Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.
- Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase.
- Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.
- HIV antibody seroprevalence among childbearing women surveyed in Maryland.
- State-sponsored genetic services in Maryland.
- Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
- Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].
- Association study of transforming growth factor alpha (TGF alpha) TaqI polymorphism and oral clefts: indication of gene-environment interaction in a population-based s...
- Immunogenicity of Haemophilus influenzae type b polysaccharide and Neisseria meningitidis outer membrane protein complex conjugate vaccine in infants and children with...
- Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for...
- Residential mobility during pregnancy: implications for environmental teratogenesis.
- Hydrops fetalis associated with Gaucher disease.
- Maternal cigarette smoking and oral clefts: a population-based study.
- Maternal, infant, and delivery factors associated with neonatal thyroid hormone status.
Schools
University of Maryland At Baltimore Professional Schools
Mass Genl Hospital
University MD Hospital
Johns Hopkins University
Johns Hopkins University Hospital
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
-
Johns Hopkins University -
University of Maryland -
Massachusetts General Hospital -
University of Maryland School of Medicine
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