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Autism severity is associated with child and maternal MAOA genotypes

Clinical genetics, 2011-04, Vol.79 (4), p.355-362

2011

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Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

Clinical genetics, 2009-02, Vol.75 (2), p.133-140

2009

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Association of autism severity with a monoamine oxidase A functional polymorphism

Clinical genetics, 2003-09, Vol.64 (3), p.190-197

2003

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Textured growth of diamond on silicon via in situ carburization and bias-enhanced nucleation

Applied physics letters, 1993-03, Vol.62 (11), p.1215-1217

1993

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Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype

European journal of medical genetics, 2005, Vol.48 (1), p.51-55

2005

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LiverClear: A versatile protocol for mouse liver tissue clearing

STAR protocols, 2022-03, Vol.3 (1), p.101178-101178, Article 101178

2022

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An improved method for detecting telomere size differences in T-lymphocyte interphases from older people with Down syndrome with and without mild cognitive impairment

Biology methods and protocols, 2017-01, Vol.2 (1), p.bpx005-bpx005

2017

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Pseudomonas aeruginosa Exotoxin A Induces Human Mast Cell Apoptosis by a Caspase-8 and -3-dependent Mechanism

The Journal of biological chemistry, 2004-08, Vol.279 (35), p.37201-37207

2004

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Adult fragile X syndrome: clinico-neuropathologic findings

Acta neuropathologica, 1985-01, Vol.67 (3-4), p.289-295

1985

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Viral pharmacovigilance study of haemophiliacs receiving porcine factor VIII

Haemophilia : the official journal of the World Federation of Hemophilia, 2002-11, Vol.8 (6), p.798-801

2002

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Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test

JAMA : the journal of the American Medical Association, 1993-10, Vol.270 (13), p.1569

1993

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Why are autism and the fragile-X syndrome associated ? conceptual and methodological issues

American journal of human genetics, 1991-02, Vol.48 (2), p.195-202

1991

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Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies

Prenatal diagnosis, 1992-07, Vol.12 (7), p.555-573

1992

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Parent-Child Dyadic Gaze Patterns in Fragile X Males and in Non-fragile X Males with Autistic Disorder

Journal of child psychology and psychiatry, 1989-11, Vol.30 (6), p.845-856

1989

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An enzyme-linked immunosorbent assay for detection of porcine parvovirus in fetal tissues

Journal of virological methods, 1992-09, Vol.39 (1), p.179-184

Jenkins, C.E.

1992

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Mitotic index and Alzheimerʼs disease

Neuroreport, 1998-12, Vol.9 (17), p.3857-3861

1998

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Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate

JIMD Reports - Volume 11, 2013, Vol.11, p.87-92

2013

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Identification of a Candidate Human Spectrin Src Homology 3 Domain-binding Protein Suggests a General Mechanism of Association of Tyrosine Kinases with the Spectrin-based Membrane Skeleton

The Journal of biological chemistry, 1998-05, Vol.273 (22), p.13681-13692

1998

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Polymerase chain reaction method to identify Down syndrome model segmentally trisomic mice

Analytical biochemistry, 2005-05, Vol.340 (2), p.213-219

2005

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Polymerase chain reaction analysis of fragile X mutations

Human genetics, 1992-09, Vol.90 (1-2), p.55-61

1992

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Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation

American journal of medical genetics, 1997-04, Vol.74 (2), p.167-171

1997

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SPARC: A Multiscale Analysis of the Structure of the Rat Lower Urinary Tract (LUT) and Connectivity of Sensory and Autonomic Nerve Terminals

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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Further evidence for genetic heterogeneity in the fragile X syndrome

Human genetics, 1987-04, Vol.75 (4), p.311-321

1987

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Fragile X syndrome: Associated neurological abnormalities and developmental disabilities

Annals of neurology, 1985-12, Vol.18 (6), p.665-669

1985

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Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

Human genetics, 1985-01, Vol.69 (3), p.209-211

1985

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Autism severity is associated with child and maternal MAOA genotypes

Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

Association of autism severity with a monoamine oxidase A functional polymorphism

Textured growth of diamond on silicon via in situ carburization and bias-enhanced nucleation

Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype

LiverClear: A versatile protocol for mouse liver tissue clearing

An improved method for detecting telomere size differences in T-lymphocyte interphases from older people with Down syndrome with and without mild cognitive impairment

Pseudomonas aeruginosa Exotoxin A Induces Human Mast Cell Apoptosis by a Caspase-8 and -3-dependent Mechanism

Adult fragile X syndrome: clinico-neuropathologic findings

Viral pharmacovigilance study of haemophiliacs receiving porcine factor VIII

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test

Why are autism and the fragile-X syndrome associated ? conceptual and methodological issues

Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies

Parent-Child Dyadic Gaze Patterns in Fragile X Males and in Non-fragile X Males with Autistic Disorder

An enzyme-linked immunosorbent assay for detection of porcine parvovirus in fetal tissues

Mitotic index and Alzheimerʼs disease

Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate

Identification of a Candidate Human Spectrin Src Homology 3 Domain-binding Protein Suggests a General Mechanism of Association of Tyrosine Kinases with the Spectrin-based Membrane Skeleton

Polymerase chain reaction method to identify Down syndrome model segmentally trisomic mice

Polymerase chain reaction analysis of fragile X mutations

Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation

SPARC: A Multiscale Analysis of the Structure of the Rat Lower Urinary Tract (LUT) and Connectivity of Sensory and Autonomic Nerve Terminals

Further evidence for genetic heterogeneity in the fragile X syndrome

Fragile X syndrome: Associated neurological abnormalities and developmental disabilities

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

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