Mouse and hamster mutants as models for Waardenburg syndromes in humans.

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

1951 • 627 citations

Mendelian Inheritance in Man

1987 • 599 citations

Gene‐induced embryological modifications of primordial germ cells in the mouse

1957 • 556 citations

Analysis of the developmental effects of a lethal mutation in the house mouse

1954 • 290 citations

Mouse DNA ‘fingerprints’: analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains

1987 • 215 citations

Maps of linkage and synteny homologies between mouse and man

1989 • 212 citations

Mouse chromosome atlas.

1990 • 194 citations

The Human Homologs of the raf ( mil ) Oncogene Are Located on Human Chromosomes 3 and 4

1984 • 177 citations

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

1981 • 174 citations

An experimental analysis of the pigment defect caused by mutations at the W and Sl loci in mice

1968 • 139 citations

Neue Mutationen und Koppelungsgruppen bei der Hausmaus

1942 • 135 citations

Report of the committee on the genetic constitution of chromosomes 7, 8, and 9.

1982 • 127 citations

Observations on the histological features, development and pathogenesis of the inner ear degeneration of the deaf white cat

1965 • 122 citations

Heterogeneity in Waardenburg syndrome.

1977 • 116 citations

Genetic heterogeneity in the Waardenburg syndrome.

1971 • 113 citations

The relationship between abnormalities of pigmentation and of the inner ear

1970 • 111 citations

MAMMALIAN GENOME ORGANIZATION: AN EVOLUTIONARY VIEW

1988 • 110 citations

Waardenburg's syndrome

1960 • 104 citations

The association of Waardenburg syndrome and Hirschsprung megacolon

1979 • 104 citations

Two closely linked genes in the mouse

1960 • 104 citations

Report of the committee on comparative mapping

1989 • 104 citations

The anomalies oe the labyrinth of the mutants varitint-waddler, shaker-2 and jerker in the mouse

1954 • 100 citations

Waardenburg's Syndrome With Fundus and Other Anomalies

1966 • 98 citations

LYSOSOMAL DYSFUNCTIONS ASSOCIATED WITH MUTATIONS AT MOUSE PIGMENT GENES

1979 • 97 citations

Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man.

1957 • 93 citations

Hereditary deafness in the Dalmatian dog

1976 • 87 citations

Pigmentary Disorders in Association With Congenital Deafness

1967 • 83 citations

Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3)

1989 • 77 citations

Historical background and evidence for dominant inheritance of the Klein‐Waardenburg syndrome (type III)

1983 • 75 citations

Hereditary Deafness in the Dalmation Dog

1962 • 66 citations

Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).

1983 • 60 citations

Upper limb involvement in the Klein-Waardenburg syndrome

1982 • 58 citations

Congenital Deafness in White Cats

1959 • 54 citations

Assignment of the AK1:Np:ABO linkage group to human chromosome 9.

1976 • 53 citations

WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.

1964 • 52 citations

LI Deaf White Mink: Electron Microscopic Study of the Inner Ear

1967 • 52 citations

The origin of the abnormalities of the inner ear in dreher mice

1964 • 51 citations

A Mutation Influencing the Transportation of Manganese, L-Dopa, and L-Tryptophan

1972 • 49 citations

The eye and skeletal effects of two mutant alleles at the microphthalmia locus of Mus musculus

1967 • 48 citations

Ophthalmological Findings in 34 Patients with Waardenburg Syndrome

1978 • 47 citations

The neural crest and the acoustic ganglion

1967 • 47 citations

STUDIES ON MEGACOLON IN PIEBALD MICE

1962 • 46 citations

THREE GENERATIONS OF DEAF WHITE CATS

1942 • 46 citations

A new oncogene, c-raf, is located on mouse chromosome 6

1984 • 44 citations

Segregation of ABO, AK₁ and ACON_S in families with abnormalities of chromosome 9

1978 • 42 citations

Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.

1989 • 42 citations

Some observations on the microphthalmia gene in the mouse

1948 • 41 citations

A case of deletion 2q35----qter and a peculiar phenotype.

1984 • 40 citations

The locus map of the mouse.

1990 • 39 citations

STUDIES ON SPOTTING PATTERNS I. ANALYSIS OF QUANTITATIVE VARIATIONS IN THE PIED SPOTTING OF THE HOUSE MOUSE

1937 • 38 citations

Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers

1977 • 38 citations

Heterogeneity in Waardenburg's Syndrome

1978 • 38 citations

Interstitial deletion of the long arm of chromosome 2: case report and review of literature.

1981 • 36 citations

Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2) (q34q36)

1976 • 35 citations

The Waardenburg syndrome.

1971 • 33 citations

Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del(2) (q31q33)

1986 • 33 citations

Interstitial deletion 2q31→q33

1983 • 32 citations

Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV

1969 • 32 citations

Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation

1983 • 31 citations

Restriction fragment length polymorphism (RFLP): applications in human chromosome mapping and genetic disease research.

1988 • 30 citations

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis

1987 • 30 citations

Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father

1983 • 29 citations

Mouse gene list.

1990 • 28 citations

Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).

1983 • 28 citations

Duplication 2q33→2q37 due to paternal ins (12;2) translocation

1978 • 27 citations

A gene triplet in the mouse

1970 • 27 citations

MUTANT WHITE MICE

1947 • 26 citations

Observations on the Histogenesis of the Inner Ear Degeneration of the Deaf White Cat and Its Possible Relationship to the Ætiology of Certain Unexplained Varieties of Human Congenital Deafness

1966 • 26 citations

Assignment of the rhodopsin gene to human chromosome 3.

1986 • 24 citations

Distal 2q duplication: Report of two familial cases and an attempt to define a syndrome

1979 • 22 citations

Genetic studies of the Syrian hamster

1964 • 21 citations

Animal models of pigment and hearing abnormalities in man.

1971 • 20 citations

GENETIC BASIS OF SOME WHITE PHENOTYPES IN THE RANCH MINK

1954 • 20 citations

Mi-spotted: a mutation in the mouse

1964 • 20 citations

A new allele of microphthalmia induced in the mouse: microphthalmia - defective iris (mi^di)

1985 • 19 citations

Waardenburg syndrome — two distinct types

1980 • 19 citations

Waardenburg syndrome—penetrance of major signs

1983 • 18 citations

Anophthalmic Albino: A New Mutation in the Syrian Hampster, Cricetus (Mesocricetus) Auratus

1958 • 17 citations

Report of the committee on the genetic constitution of chromosomes 7, 8 and 9

1987 • 17 citations

The Histopathology of Hereditary Congenital Deafness in White Mink

1965 • 16 citations

Waardenburg's Syndrome in Six Generations of One Family

1965 • 16 citations

Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits

1974 • 13 citations

LINKAGE STUDIES IN A NEW BLACK-EYED WHITE MUTATION

1957 • 13 citations

Probable loose linkage between the AB0 locus and Waardenburg syndrome type I

1975 • 11 citations

Effects of pinealectomy on reproduction in the Syrian hamster mutant anophthalmic white (Wh)

1983 • 11 citations

A new allele at the patch locus in the mouse

1977 • 11 citations

The primary ultrastructural defect caused by anophthalmic white (Wh) in the Syrian hamster.

1982 • 10 citations

Waardenburg's Syndrome: Variations in Expressivity

1981 • 9 citations

Anophthalmic White: A Mutant with Unusual Morphological and Pigmentary Properties in the Syrian Hamster

1962 • 9 citations

Current status of the ABO-Waardenburg syndrome type I linkage

1978 • 9 citations

Das Waardenburg-Syndrom, dargestellt an f�nf Familien

1965 • 8 citations

Effects of the gene Wh on reproduction in the Syrian hamster, Mesocricetus auratus

1980 • 8 citations

An Association of Hereditary Eye Defects with White Spotting

1952 • 7 citations

Concerning the primary defect leading to the pleiotropic effects caused by anophthalmic white (Wh) in the Syrian hamster Mesocricetus auratus

1981 • 7 citations

A Partial Dominant for Suppression of Color in the Syrian Hamster, Cricetus Mesocricetus auratus

1959 • 7 citations

A histological examination of the pars distalis from the syrian hamster mutant anophthalmic white (Wh)

1981 • 5 citations

Site of gene action of the white allele (Mi^wh) of the microphthalmia locus: A dermal‐epidermal recombination study

1982 • 5 citations

Waardenburg’s syndrome

1969 • 3 citations

An analysis of the phenotype and gene action of microphthalmic white (Miwh) in the house mouse.

1980 • 3 citations

WHITESIDE, A NEW MUTATION IN PEROMYSCUS

1956 • 2 citations

WAARDENBURGʼS SYNDROME

1964 • 1 citations

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