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Results: 1-7 |
Results: 7
A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22
Authors: FELDMAN GJ WARD DE LAJEUNIERENIER E SAAVEDRA D ROBIN NH PROUD V ROBB LJ KALOUSTIAN VD CAREY JC COHEN MM CORMIER V MUNNICH A ZACKAI EH WILKIE AOM PRICE RA MUENKE M
Citation: Gj. Feldman et al., A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22, Human molecular genetics, 6(11), 1997, pp. 1937-1941
DETERMINATION OF THE GENOMIC STRUCTURE OF THE XNP ATRX GENE ENCODING A POTENTIAL ZINC-FINGER HELICASE/
Authors: VILLARD L LOSSI AM CARDOSO C PROUD V CHIARONI P COLLEAUX L SCHWARTZ C FONTES M
Citation: L. Villard et al., DETERMINATION OF THE GENOMIC STRUCTURE OF THE XNP ATRX GENE ENCODING A POTENTIAL ZINC-FINGER HELICASE/, Genomics, 43(2), 1997, pp. 149-155
GENETIC TESTING OF CHILDREN AT RISK FOR HUNTINGTONS-DISEASE
Authors: NANCE MA ABRAMSON R ASHIZAWA T CODORI AM FOX M GETTIG B MYERS RH QUAID K SELTZER W SHEA DK WEXLER N ZANKO A PROUD V RICHTER S HAUCK L BROOME D BASS H JONES OW ZANKO A BODELL A TAYLOR L HAVERKAMP C HEIMLER A DIMAIO M HAUN R DIAMOND T JONES R YIM D DONLON S EVERS C SHANNON K LEBEL R POLZIN S MILLER J QUAID K GRAY C GODFREY N MYERS R UHLMANN W LUDOWESE C LEROY B OTTO E JOHNSON J MCCORMACK M COPE J PALLADINO L LEWIS J MCKENNA C HICKEY C THOMSON L WATERSON J HUELSMAN K LINARD S SCHAEFER F RUBENSTEIN J KOVAK K GOODWIN D GODMILOW L SCHRAMKE C SKOREYSOLLBERG P POTTER N HANNIG V BROOKSHIRE G HELLER K KESTER M LEONARD K MENGDEN GA BATY B ALLINSON P BENNETT R HINER B GOONEWARDENA P SPECTOR E MCINTOSH N MUELLER OT SHOFFNER J BERRYKRAVIS E DEMARCHI J KASCH L MATTHIASHAGEN V BARTHOLOMEW D PRIOR T SCHAEFER F GOODWIN D VNENCAKJONES C POTTER N RICHARDS S
Citation: Ma. Nance et al., GENETIC TESTING OF CHILDREN AT RISK FOR HUNTINGTONS-DISEASE, Neurology, 49(4), 1997, pp. 1048-1053
NOVEL X-LINKED INHERITANCE PATTERN IN CRANIOFRONTONASAL SYNDROME
Authors: FELDMAN GJ WARD DE ROBIN NH ARONSON AL ZACKAI UH SAAVEDRA D PROUD V ROBB LJ KALOUSTIAN V JABS E CAREY JC MUNNICH A COHEN MM PRICE RA MUENKE M
Citation: Gj. Feldman et al., NOVEL X-LINKED INHERITANCE PATTERN IN CRANIOFRONTONASAL SYNDROME, Journal of dental research, 76, 1997, pp. 3073-3073
A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22
Authors: MUENKE M FELDMAN GJ WARD DE LAJEUNIERENIER E SAAVEDRA D ROBIN NH PROUD V ROBB LJ KALOUSTIAN VD CAREY JC COHEN MM CORMIER V MUNNICH A ZACKAI EH WILKIE AOM PRICE RA
Citation: M. Muenke et al., A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22, American journal of human genetics, 61(4), 1997, pp. 255-255
X-LINKED LETHAL INFANTILE SPINAL MUSCULAR-ATROPHY (XL-SMA) - ADDITIONAL CLINICAL AND MOLECULAR STUDIES SUPPORT A DISEASE LOCUS AT XP11.3-Q11.2
Authors: BAUMBACH L YANG T CLARK RD GEORGE A PROUD V HOFFMAN E
Citation: L. Baumbach et al., X-LINKED LETHAL INFANTILE SPINAL MUSCULAR-ATROPHY (XL-SMA) - ADDITIONAL CLINICAL AND MOLECULAR STUDIES SUPPORT A DISEASE LOCUS AT XP11.3-Q11.2, American journal of human genetics, 61(4), 1997, pp. 1554-1554
POOLING STRATEGIES AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES - STUDIES IN LATTICE, GRANULAR AND AVELLINO DYSTROPHIES
Authors: KANIS AB MATHERS WD HOLLAND EJ ROSENWASSER GOD ROSA N KIM W PROUD V LAM B SHEFFIELD VC STONE EM
Citation: Ab. Kanis et al., POOLING STRATEGIES AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES - STUDIES IN LATTICE, GRANULAR AND AVELLINO DYSTROPHIES, Investigative ophthalmology & visual science, 36(4), 1995, pp. 771-771
Risultati: 1-7 |