J. Schuette

发表

CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype

C. Keegan, M. Stem, C. Besirli, 2016, Ophthalmic genetics.

Novel DICER1 mutation as cause of multinodular goiter in children

J. Bedoyan, M. Lesperance, J. Schuette, 2013, Head & neck.

Evidence for Mass Flow in Flowering Individuals of the Submersed Vascular Plant Myriophyllum heterophyllum

M. Klug, J. Schuette, 1995, Plant physiology.

Duplication 2p25 in a child with clinical features of CHARGE syndrome

D. M. Martin, C. V. van Ravenswaaij-Arts, G. Green, 2016, American journal of medical genetics. Part A.

Electroweak parameters of the Z$^0$ resonance and the standard model

P. K. Malhotra, N. C. Wood, P. G. Verdini, 1991 .

Mass limits for excited electrons and muons from Z0 decay

P. K. Malhotra, J. Y. Li, B. Roe, 1990 .

Measurement of g(A) and g(V), the neutral current coupling constants to leptons

B. Roe, C. Dionisi, C. Luci, 1990 .

Parents’ Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis

B. Yashar, K. Owens, L. Kiedrowski, 2016, Journal of Genetic Counseling.

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

Edward Yang, Laurence Faivre, Jillian S Parboosingh, 2015, American journal of human genetics.

Yield of Additional Genetic Testing after Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

S. Schwartz, David T. Miller, C. Morton, 2018, Genetics in Medicine.

Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

S. Schwartz, David T. Miller, C. Martin, 2018, Genetics in Medicine.

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Neil H. Parker, Dylan M. Marchione, R. Redon, 2020, Science Advances.

Who Counsels Parents of Newborns Who Are Carriers of Sickle Cell Anemia or Cystic Fibrosis?

Kathryn L. Moseley, A. Campbell, S. Nasr, 2013, Journal of Genetic Counseling.

Anatomical analysis of growth and developmental patterns in the internode of deepwater rice

A. Bleecker, H. Kende, H. Kende, 1986, Planta.

A guide to genetic counseling

B. Yashar, W. Uhlmann, Jane L. Schuette, 1998 .

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.

Matthew H. Brush, David R. Murdock, Jean M. Davidson, 2019, Biological psychiatry.

Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome.

Jay Shendure, Michael J Bamshad, Deborah A Nickerson, 2012, American journal of human genetics.

Guidelines for Writing Letters to Patients

W. Uhlmann, Diane L. Baker, Timothy Eash, 2002, Journal of Genetic Counseling.

Lacunar pressures in Myriophyllum heterophyllum: manometric measurement and diurnal gas dynamics in field populations

J. Schuette, 1996 .

Influence of stem lacunar structure on gas transport: relation to the oxygen transport potential of submersed vascular plants

M. Klug, J. Schuette, K. Klomparens, 1994 .