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Results: 1-19 |
Results: 19
XL-ALPHA-S IS A PATERNALLY DERIVED PROTEIN PRODUCT OF THE HUMAN GNAS1GENE
Authors: HAYWARD B KAMIYA M TAKADA S MORAN V STRAIN L HAYASHIZAKI Y BONTHRON DT
Citation: B. Hayward et al., XL-ALPHA-S IS A PATERNALLY DERIVED PROTEIN PRODUCT OF THE HUMAN GNAS1GENE, European journal of human genetics, 6, 1998, pp. 305-305
A TRUE HERMAPHRODITE CHIMERA RESULTING FROM EMBRYO AMALGAMATION AFTERIN-VITRO FERTILIZATION
Authors: STRAIN L DEAN JCS HAMILTON MPR BONTHRON DT
Citation: L. Strain et al., A TRUE HERMAPHRODITE CHIMERA RESULTING FROM EMBRYO AMALGAMATION AFTERIN-VITRO FERTILIZATION, The New England journal of medicine, 338(3), 1998, pp. 166-169
THE HUMAN GNAS1 GENE IS IMPRINTED AND ENCODES DISTINCT PATERNALLY ANDBIALLELICALLY EXPRESSED G-PROTEINS
Authors: HAYWARD BE KAMIYA M STRAIN L MORAN V CAMPBELL R HAYASHIZAKI Y BONTHRON DT
Citation: Be. Hayward et al., THE HUMAN GNAS1 GENE IS IMPRINTED AND ENCODES DISTINCT PATERNALLY ANDBIALLELICALLY EXPRESSED G-PROTEINS, Proceedings of the National Academy of Sciences of the United Statesof America, 95(17), 1998, pp. 10038-10043
KERATOSIS-FOLLICULARIS SPINULOSA DECALVANS - CONFIRMATION OF LINKAGE TO XP22.13-P22.2
Authors: PORTEOUS MEM STRAIN L LOGIE LJ HERD RM BENTON EC
Citation: Mem. Porteous et al., KERATOSIS-FOLLICULARIS SPINULOSA DECALVANS - CONFIRMATION OF LINKAGE TO XP22.13-P22.2, Journal of Medical Genetics, 35(4), 1998, pp. 336-337
NEUROGENIC CHRONIC IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION, PATENT DUCTUS-ARTERIOSUS, AND THROMBOCYTOPENIA SEGREGATING AS AN X-LINKED RECESSIVE DISORDER
Authors: FITZPATRICK DR STRAIN L THOMAS AE BARR DGD TODD A SMITH NM SCOBIE WG
Citation: Dr. Fitzpatrick et al., NEUROGENIC CHRONIC IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION, PATENT DUCTUS-ARTERIOSUS, AND THROMBOCYTOPENIA SEGREGATING AS AN X-LINKED RECESSIVE DISORDER, Journal of Medical Genetics, 34(8), 1997, pp. 666-669
FRIED-SYNDROME IS A DISTINCT X-LINKED MENTAL-RETARDATION SYNDROME MAPPING TO XP22
Authors: STRAIN L WRIGHT AF BONTHRON DT
Citation: L. Strain et al., FRIED-SYNDROME IS A DISTINCT X-LINKED MENTAL-RETARDATION SYNDROME MAPPING TO XP22, Journal of Medical Genetics, 34(7), 1997, pp. 535-540
EMBRYO AMALGAMATION AFTER IN-VITRO FERTILIZATION, RESULTING IN A TRUEHERMAPHRODITE CHIMERA
Authors: BONTHRON D STRAIN L DEAN JCS
Citation: D. Bonthron et al., EMBRYO AMALGAMATION AFTER IN-VITRO FERTILIZATION, RESULTING IN A TRUEHERMAPHRODITE CHIMERA, Journal of Medical Genetics, 34, 1997, pp. 37-37
FRAGILE-X-SYNDROME RESULTING FROM A DELETION OF THE FMR1 GENE
Authors: MOORE S DEAN JCS COLE GF HAMILTON L KELLY KF STRAIN L WARNER J
Citation: S. Moore et al., FRAGILE-X-SYNDROME RESULTING FROM A DELETION OF THE FMR1 GENE, Journal of Medical Genetics, 34, 1997, pp. 541-541
AMALGAMATION OF IN-VITRO FERTILIZED EMBRYOS, RESULTING IN BIRTH OF A TRUE HERMAPHRODITE CHIMERA
Authors: BONTHRON DT STRAIN L DEAN JCS
Citation: Dt. Bonthron et al., AMALGAMATION OF IN-VITRO FERTILIZED EMBRYOS, RESULTING IN BIRTH OF A TRUE HERMAPHRODITE CHIMERA, American journal of human genetics, 61(4), 1997, pp. 841-841
DISCORDANT SEGREGATION OF XQ28 MARKERS AND A MUTATION IN THE L1 GENE IN A FAMILY WITH X-LINKED HYDROCEPHALUS
Authors: JOUET M STRAIN L BONTHRON D KENWRICK S
Citation: M. Jouet et al., DISCORDANT SEGREGATION OF XQ28 MARKERS AND A MUTATION IN THE L1 GENE IN A FAMILY WITH X-LINKED HYDROCEPHALUS, Journal of Medical Genetics, 33(3), 1996, pp. 248-250
A HUMAN PARTHENOGENETIC CHIMERA
Authors: STRAIN L WARNER JP JOHNSTON T BONTHRON DT
Citation: L. Strain et al., A HUMAN PARTHENOGENETIC CHIMERA, Nature genetics, 11(2), 1995, pp. 164-169
A HUMAN PARTHENOGENETIC CHIMERA
Authors: STRAIN L WARNER JP JOHNSTON T BONTHRON DT
Citation: L. Strain et al., A HUMAN PARTHENOGENETIC CHIMERA, American journal of human genetics, 57(4), 1995, pp. 780-780
PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION
Authors: STRAIN L PORTEOUS MEM GOSDEN CM ELLIS PM NEILSON JP BONTHRON DT
Citation: L. Strain et al., PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION, Prenatal diagnosis, 14(6), 1994, pp. 469-474
PRENATAL-DIAGNOSIS OF X-LINKED HYDROCEPHALUS
Authors: STRAIN L BROCK DJH BONTHRON DT
Citation: L. Strain et al., PRENATAL-DIAGNOSIS OF X-LINKED HYDROCEPHALUS, Prenatal diagnosis, 14(5), 1994, pp. 415-416
GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - A FAMILY SHOWING LINKAGE TO MARKERS IN XQ27.3
Authors: STRAIN L BROCK DJH BONTHRON DT
Citation: L. Strain et al., GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - A FAMILY SHOWING LINKAGE TO MARKERS IN XQ27.3, Journal of Medical Genetics, 31(2), 1994, pp. 167-168
PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION
Authors: STRAIN L PORTEOUS MEM BONTHRON DT
Citation: L. Strain et al., PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION, Journal of Medical Genetics, 31(2), 1994, pp. 170-170
HETEROGENEITY ANALYSIS IN 40 X-LINKED RETINITIS-PIGMENTOSA FAMILIES
Authors: TEAGUE PW ALDRED MA JAY M DEMPSTER M HARRISON C CAROTHERS AD HARDWICK LJ EVANS HJ STRAIN L BROCK DJH BUNDEY S JAY B BIRD AC BHATTACHARYA SS WRIGHT AF
Citation: Pw. Teague et al., HETEROGENEITY ANALYSIS IN 40 X-LINKED RETINITIS-PIGMENTOSA FAMILIES, American journal of human genetics, 55(1), 1994, pp. 105-111
GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - LINKAGE TO MARKERS WITHIN XQ27.3
Authors: STRAIN L GOSDEN CM BROCK DJH BONTHRON DT
Citation: L. Strain et al., GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - LINKAGE TO MARKERS WITHIN XQ27.3, American journal of human genetics, 54(2), 1994, pp. 236-243
GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - LINKAGE OF HSAS2 TOMARKERS IN XQ27.3
Authors: STRAIN L BROCK DJH BONTHRON DT
Citation: L. Strain et al., GENETIC-HETEROGENEITY IN X-LINKED HYDROCEPHALUS - LINKAGE OF HSAS2 TOMARKERS IN XQ27.3, American journal of human genetics, 53(3), 1993, pp. 1084-1084
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