scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF00591074 |
P698 | PubMed publication ID | 3469136 |
P2093 | author name string | J L Haines | |
P M Conneally | |||
J C Christian | |||
M E Hodes | |||
S R Dlouhy | |||
P2860 | cites work | Strategies for multilocus linkage analysis in humans | Q27860521 |
A familial syndrome of short stature associated with facial dysplasia and genital anomalies | Q28253439 | ||
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 studies | Q35570490 | ||
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency | Q37686181 | ||
The FG syndrome: Further characterization, report of a third family, and of a sporadic case | Q41035045 | ||
The genetic linkage map of the human X chromosome | Q45890080 | ||
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 retardation | Q52110942 | ||
Assignment of the gene for dyskeratosis congenita to Xq28 | Q56797967 | ||
DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA | Q69106586 | ||
Congenital familial testicular deficiency | Q73088600 | ||
P433 | issue | 2 | |
P304 | page(s) | 136-139 | |
P577 | publication date | 1987-02-01 | |
P1433 | published in | Human Genetics | Q5937167 |
P1476 | title | Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter. | |
P478 | volume | 75 |
Q36953295 | A genome wide linkage scan of metacarpal size and geometry in the Framingham Study |
Q35443982 | A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27. |
Q50907815 | A whole genome linkage scan for QTLs underlying peak bone mineral density. |
Q68296917 | Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome) |
Q52040978 | Linkage to Xq28 in a family with nonspecific X-linked mental retardation |
Q33597042 | Localisation of the MRX3 gene for non-specific X linked mental retardation |
Q47820674 | Ocular manifestations in the X-linked intellectual disability syndromes |
Q67941705 | X linked mental retardation |
Q51983447 | X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. |
Search more.