Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

scientific article published in February 1987

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF00591074
P698PubMed publication ID3469136

P2093author name stringJ L Haines
P M Conneally
J C Christian
M E Hodes
S R Dlouhy
P2860cites workStrategies for multilocus linkage analysis in humansQ27860521
A familial syndrome of short stature associated with facial dysplasia and genital anomaliesQ28253439
Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.Q34207831
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.Q35200306
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studiesQ35570490
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyQ37686181
The FG syndrome: Further characterization, report of a third family, and of a sporadic caseQ41035045
The genetic linkage map of the human X chromosomeQ45890080
Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).Q52090614
Conference report: International Workshop on the fragile X and X-linked mental retardation.Q52093774
X-linked skeletal dysplasia with mental retardationQ52110942
Assignment of the gene for dyskeratosis congenita to Xq28Q56797967
DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNAQ69106586
Congenital familial testicular deficiencyQ73088600
P433issue2
P304page(s)136-139
P577publication date1987-02-01
P1433published inHuman GeneticsQ5937167
P1476titleLocalization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.
P478volume75

Reverse relations

cites work (P2860)
Q36953295A genome wide linkage scan of metacarpal size and geometry in the Framingham Study
Q35443982A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27.
Q50907815A whole genome linkage scan for QTLs underlying peak bone mineral density.
Q68296917Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome)
Q52040978Linkage to Xq28 in a family with nonspecific X-linked mental retardation
Q33597042Localisation of the MRX3 gene for non-specific X linked mental retardation
Q47820674Ocular manifestations in the X-linked intellectual disability syndromes
Q67941705X linked mental retardation
Q51983447X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.

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