A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter.

scientific article published in May 1988

A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/AJMG.1320300153
P698PubMed publication ID3177468

P2093author name stringSutherland GR
Turner G
Partington MW
Mulley JC
Thode A
P2860cites workA New Dominant Gene Mental Retardation SyndromeQ56505393
P433issue1-2
P304page(s)509-521
P577publication date1988-05-01
P1433published inAmerican Journal of Medical Genetics Part AQ15755121
P1476titleA family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter.
P478volume30

Reverse relations

cites work (P2860)
Q33680152"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome
Q34811039Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes
Q34152932Coffin-Lowry syndrome: clinical and molecular features
Q35195476Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
Q37220081Forty years from markers to genes
Q68298877Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region
Q48391546Isolated neurodevelopmental delay in childhood: Clinicoradiological correlation in 170 patients
Q42331611Mechanical ventilation in Coffin-Lowry syndrome: a case report
Q45961186Postmortem findings in the Coffin-Lowry Syndrome.
Q36682803Signal transduction mechanisms in memory disorders
Q34306122Splitting and lumping in the nosology of XLMR.
Q49874678The natural history of spinal deformity in patients with Coffin-Lowry syndrome
Q73013123X-linked mental retardation

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