J. F. Arena

发表

Characterizing the Pattern of Anomalies in Congenital Zika Syndrome for Pediatric Clinicians

S. Rasmussen, C. Moore, W. Dobyns, 2017, JAMA pediatrics.

Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research.

Rui Mei, Hui-Ju Tsai, Elad Ziv, 2005, American journal of public health.

In response to “In utero exposure to methotrexate and risk of congenital malformations”

J. Reefhuis, Tiffany J. Riehle‐Colarusso, J. F. Arena, 2015, American journal of medical genetics. Part A.

Localization to Xq22 and clinical update of a family with X-linked recessive mental retardation with progression sensorineural deafness, progressive tapeto-retinal degeneration and dystonia

R. Stevenson, C. Schwartz, S. Mellgren, 1994 .

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

Robert M. Plenge, Huntington F. Willard, Anna Naumova, 1997, Nature Genetics.

Maternal exposure to methotrexate and birth defects: A population‐based study

J. Reefhuis, Tiffany J. Riehle‐Colarusso, J. F. Arena, 2014, American journal of medical genetics. Part A.

X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.

R. Stevenson, C. Schwartz, H. Lubs, 1999, American journal of medical genetics.

A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25

R. Stevenson, C. Schwartz, H. Lubs, 2000, Journal of medical genetics.

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Hanlee P. Ji, M. King, K. Heimdal, 1997, American journal of human genetics.

Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.

R. Stevenson, C. Schwartz, H. Lubs, 1992, American journal of medical genetics.

Nonsyndromic X‐linked mental retardation: review and mapping of MRX29 to Xp21

R. Stevenson, H. Lubs, R. Schroer, 1996, Clinical genetics.

X-linked mental retardation: the early era from 1943 to 1969.

R. Stevenson, C. Schwartz, H. Lubs, 1994, American journal of medical genetics.

Renpenning syndrome maps to Xp11.

R. Stevenson, C. Schwartz, H. Lubs, 1998, American journal of human genetics.

X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12.

R. Stevenson, C. Schwartz, H. Lubs, 1996, American journal of medical genetics.

Computerized approach to X-linked mental retardation syndromes.

H. Lubs, J. F. Arena, 1991, American journal of medical genetics.

Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22.

R. Stevenson, C. Schwartz, H. Lubs, 1999, American journal of medical genetics.

X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23.

R. Stevenson, C. Schwartz, H. Lubs, 1999, American journal of medical genetics.

A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

R. Stevenson, C. Schwartz, H. Lubs, 1997, Journal of medical genetics.

Study of X-linked mental retardation (XLMR): summary of 61 families in the Miami/Greenwood Study.

R. Stevenson, C. Schwartz, H. Lubs, 1996, American journal of medical genetics.

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

D. Ledbetter, J. Ott, T. Lehner, 1992, American journal of medical genetics.

Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

R. Stevenson, C. Schwartz, H. Lubs, 1997, Journal of medical genetics.

Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.

R. Stevenson, C. Schwartz, H. Lubs, 1994, American journal of medical genetics.