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A new gene (DYX3) for dyslexia is located on chromosome 2

Journal of medical genetics, 1999-09, Vol.36 (9), p.664-669

1999

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Renpenning syndrome comes into focus

American journal of medical genetics. Part A, 2005-05, Vol.134A (4), p.415-421

2005

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Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene

Clinical genetics, 2002-02, Vol.61 (2), p.139-145

2002

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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

Journal of medical genetics, 2007-07, Vol.44 (7), p.472-477

2007

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A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58

Journal of medical genetics, 2002-06, Vol.39 (6), p.430-433

2002

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

Journal of medical genetics, 2000-09, Vol.37 (9), p.663-668

2000

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Contrast sensitivity in dyslexia

Visual neuroscience, 1995-01, Vol.12 (1), p.153-163

1995

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Renpenning Syndrome Maps to Xp11

American journal of human genetics, 1998-05, Vol.62 (5), p.1092-1101

1998

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

Clinical genetics, 1996-10, Vol.50 (4), p.176-183

1996

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

Journal of medical genetics, 1997-07, Vol.34 (7), p.529-534

1997

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

Journal of medical genetics, 1997-06, Vol.34 (6), p.465-469

1997

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Cytogenetic results from the U.S. collaborative study on CVS

Prenatal diagnosis, 1992-05, Vol.12 (5), p.317-345

1992

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A marker X chromosome

American journal of human genetics, 1969-05, Vol.21 (3), p.231-244

Lubs, H A

1969

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The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities

The New England journal of medicine, 1989-03, Vol.320 (10), p.609-617

1989

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XLMR genes: Update 1990

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.186-189

1991

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Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 ( MCT8) Gene

American journal of human genetics, 2005-07, Vol.77 (1), p.41-53

2005

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Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study

Science (American Association for the Advancement of Science), 1970-07, Vol.169 (3944), p.495-497

1970

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Gender Differences in the Severity of Adult Familial Dyslexia

Reading & writing, 1995-06, Vol.7 (2), p.155-161

Feldman, E

1995

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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

Human molecular genetics, 2005-04, Vol.14 (8), p.1019-1027

2005

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Suggestive linkage of developmental dyslexia to chromosome 1p34-p36

The Lancet (British edition), 1993-07, Vol.342 (8864), p.178-178

1993

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Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders

American journal of human genetics, 2002-07, Vol.71 (1), p.168-173

2002

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Chromosome Polymorphism in American Negro and White Populations

Nature (London), 1971-09, Vol.233 (5315), p.134-136

1971

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Human Q and C chromosomal variations: distribution and incidence

Cytogenetic and genome research, 1975-01, Vol.14 (2), p.97-115

1975

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Racial differences in the frequency of Q and C chromosomal heteromorphisms

Nature (London), 1977-08, Vol.268 (5621), p.631-633

1977

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Specific Reading Disability: Identification of an Inherited Form through Linkage Analysis

Science (American Association for the Advancement of Science), 1983-03, Vol.219 (4590), p.1345-1347

1983

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A new gene (DYX3) for dyslexia is located on chromosome 2

Renpenning syndrome comes into focus

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58

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

Contrast sensitivity in dyslexia

Renpenning Syndrome Maps to Xp11

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

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

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

Cytogenetic results from the U.S. collaborative study on CVS

A marker X chromosome

The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities

XLMR genes: Update 1990

Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 ( MCT8) Gene

Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study

Gender Differences in the Severity of Adult Familial Dyslexia

A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36

Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders

Chromosome Polymorphism in American Negro and White Populations

Human Q and C chromosomal variations: distribution and incidence

Racial differences in the frequency of Q and C chromosomal heteromorphisms

Specific Reading Disability: Identification of an Inherited Form through Linkage Analysis

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