S. Panny

发表

Birth Delivery Mode Modifies the Associations between Prenatal Polychlorinated Biphenyl (PCB) and Polybrominated Diphenyl Ether (PBDE) and Neonatal Thyroid Hormone Levels

L. Goldman, B. Apelberg, F. Witter, 2008, Environmental health perspectives.

Folic Acid for the Prevention of Neural Tube Defects

C. Moore, B. Pletcher, C. Cunniff, 1999, Pediatrics.

US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN).

P. Fernhoff, L. Elsas, J. Parks, 2000, The Journal of pediatrics.

Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) method.

A. Moser, G. Raymond, D. Macaya, 2009, Molecular genetics and metabolism.

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 Genetic Services.

Michael R. Glass, E. McCabe, W. H. Hannon, 1996, Biochemical and molecular medicine.

U.S. newborn screening system guidelines: Statement of the council of regional networks for genetic services

E. McCabe, W. H. Hannon, A. Davidson, 1992 .

A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta

S. Tishkoff, C. Rotimi, A. Adeyemo, 2012, Genetics in Medicine.

Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies.

G. Shaw, M. Khoury, L. Edmonds, 1996, American journal of medical genetics.

Molecular genetic testing in pediatric practice: A subject review. Committee on Genetics.

H. Hoyme, C. Moore, J. Moeschler, 2016, Pediatrics.

Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.

A. F. Scott, H. Kazazian, C. Boehm, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Characteristics influencing informed consent on a congenital malformations registry.

M. O. Robertson, S. Panny, C. Law, 1988, American journal of public health.

A complex rearrangement, including a deleted 8q, in a case of Langer‐Giedion syndrome

S. Schwartz, M. Cohen, S. Panny, 1985, Clinical genetics.

Residential mobility during pregnancy: implications for environmental teratogenesis.

M. Khoury, W. Stewart, S. Panny, 1988, Journal of clinical epidemiology.

Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

A. F. Scott, H. Kazazian, C. Boehm, 1981, American journal of human genetics.

Hydrops fetalis associated with Gaucher disease.

S. Panny, C. C. Sun, J. Combs, 1984, Pathology, research and practice.

False Negative Cystic Fibrosis Newborn Screen

A. Hamosh, J. Collaco, P. Mogayzel, 2010, Clinical pediatrics.

Newborn screening for X-linked adrenoleukodystrophy: further evidence high throughput screening is feasible.

A. Moser, G. Raymond, W. Hubbard, 2014, Molecular genetics and metabolism.

Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase.

S. Schwartz, M. Cohen, S. Panny, 1984, American journal of human genetics.

Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996.

T. Beaty, C. Tifft, J. Hetmanski, 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Evaluation of the Newborn With Developmental Anomalies of the External Genitalia

J. Moeschler, C. Kaye, C. Cunniff, 2000, Pediatrics.

A temperature sensitive mutation of the β′‐subunit of DNA‐dependent RNA polymerase from E. coli T16

W. Zillig, S. Panny, P. Palm, 1974, FEBS letters.

Cebocephaly‐holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter→q32:)]

S. Schwartz, J. Opitz, S. Panny, 1983 .

American Academy of Pediatrics: Health care supervision for children with Williams syndrome.

J. Moeschler, C. Kaye, C. Cunniff, 2001, Pediatrics.

HIV antibody seroprevalence among childbearing women surveyed in Maryland.

E. Israel, S. Panny, J. Patel, 1990, Public health reports.

Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.

S. Schwartz, M. Cohen, M. Schwartz, 1986, American journal of human genetics.

Maternal, infant, and delivery factors associated with neonatal thyroid hormone status.

L. Goldman, B. Apelberg, F. Witter, 2008, Thyroid : official journal of the American Thyroid Association.

Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.

S. Schwartz, M. Cohen, S. Panny, 1985, American journal of medical genetics.

A case-control study of nonsyndromic oral clefts in Maryland.

T. Beaty, J. Hetmanski, Y. Chiu, 2001, Annals of epidemiology.

Association study of transforming growth factor alpha (TGF alpha) TaqI polymorphism and oral clefts: indication of gene-environment interaction in a population-based sample of infants with birth defects.

T H Beaty, T. Beaty, Shih-Jen Hwang, 1995, American journal of epidemiology.

Maternal cigarette smoking and oral clefts: a population-based study.

N. Holtzman, M. Khoury, S. Panny, 1987, American journal of public health.

Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency.

T. Beaty, T. Hefferon, S. Hwang, 1998, American journal of medical genetics.

Epidemiology of sentinel birth defects in Maryland, 1984.

M. O. Robertson, N. Holtzman, M. Khoury, 1986, Maryland medical journal.