(Q41647578)

6 October 2017

title

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics (English)

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6 October 2017

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15

Opitz J

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6 October 2017

Curry CJ

1

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6 October 2017

Stevenson RE

2

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6 October 2017

Aughton D

3

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6 October 2017

Byrne J

4

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6 October 2017

Carey JC

5

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6 October 2017

Cassidy S

6

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6 October 2017

Cunniff C

7

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6 October 2017

Graham JM Jr

8

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6 October 2017

Jones MC

9

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6 October 2017

Kaback MM

10

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6 October 2017

Moeschler J

11

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6 October 2017

Schaefer GB

12

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6 October 2017

Schwartz S

13

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6 October 2017

Tarleton J

14

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6 October 2017

publication date

1 November 1997

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American Journal of Medical Genetics Part A

6 October 2017

published in

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6 October 2017

volume

72

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6 October 2017

issue

4

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6 October 2017

page(s)

468-477

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publication type of scholarly work

6 October 2017

review article

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Frequency of the fragile X syndrome in Japanese mentally retarded males

cites work

1 reference

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Southern Child Neurology Society meeting invited lecture. The saga of the septum pellucidum: a tale of unfunded clinical investigations

21 January 2018

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Macrocrania and megalencephaly in the neonate

21 January 2018

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Evaluation of the patient with idiopathic mental retardation

21 January 2018

1 reference

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Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

21 January 2018

1 reference

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The brain and mental retardation

21 January 2018

1 reference

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Miller-Dieker syndrome: lissencephaly and monosomy 17p.

21 January 2018

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Magnetic resonance imaging in the malformative syndromes with mental retardation

21 January 2018

1 reference

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A simplified six-item checklist for screening for fragile X syndrome in the pediatric population

21 January 2018

1 reference

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Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

21 January 2018

1 reference

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An etiological survey of the severely retarded Hertfordshire children who were born between January 1, 1965 and December 31, 1967

21 January 2018

1 reference

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Value of computerised tomography in children with non-specific mental subnormally

21 January 2018

1 reference

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21 January 2018

XLMR genes: update 1996.

1 reference

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Diagnostic yield of the neurologic assessment of the developmentally delayed child

21 January 2018

1 reference

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A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

1 reference

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Evaluation of the Child with Idiopathic Mental Retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Quantitative morphometric analysis of brain growth using magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Contribution of magnetic resonance imaging to the knowledge of CNS malformations related to chromosomal aberrations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Population incidence and segregation ratios in the Martin-Bell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Asymmetry and skin pigmentary anomalies in chromosome mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

Chromosomal and biochemical screening on mentally retarded school children in Taiwan

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971112%2972%3A4%3C468%3A%3AAID-AJMG18%3E3.0.CO%3B2-P

10.1002/(SICI)1096-8628(19971112)72:4<468::AID-AJMG18>3.0.CO;2-P

21 January 2018

Identifiers

DOI

1 reference

6 October 2017

1 reference