Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions

Disruption of insulin–like growth factor 2 imprinting in Beckwith–Wiedemann syndrome

1993 • 427 citations

Catalogue of Unbalanced Chromosome Aberrations in Man

1985 • 420 citations

Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.

1991 • 385 citations

Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding

1984 • 240 citations

Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes

1988 • 106 citations

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

1992 • 104 citations

Deletions of different segments of the long arm of chromosome 4

1981 • 94 citations

Possible Localization of Gc-System on Chromosome 4. Loss of Long Arm 4 Material Associated with Father-Child Incompatibility Within the Gc-System

1977 • 87 citations

Evidence that Rieger syndrome maps to 4q25 or 4q27.

1992 • 57 citations

Tentative assignment of piebald trait gene to chromosome band 4q12

1986 • 54 citations

Interstitial deletion of the long arm of chromosome 4

1988 • 46 citations

Interstitial deletion 4q and Rieger syndrome

1981 • 44 citations

Piebald trait in a retarded child with interstitial deletion of chromosome 4.

1977 • 41 citations

Interstitial deletion of the distal long arm of chromosome 4.

1992 • 39 citations

Interstitial deletion of the proximal long arm of chromosome 4 associated with father‐child incompatibility within the Gc‐ system: Probable reduced gene dosage effect and partial piebald trait

1989 • 37 citations

Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Rieger anomaly

1995 • 31 citations

Partial trisomy 12q: a clinically recognisable syndrome. Genetic risks associated with translocations of chromosome 12q.

1983 • 30 citations

Deletion 5q35.3

1994 • 28 citations

Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.

1988 • 28 citations

A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4

1988 • 26 citations

Piebaldism in a Mentally Retarded Girl With Rare Deletion of the Long Arm of Chromosome 4

1993 • 21 citations

Partial monosomy of long arm of chromosome 4 due to interstitial deletion

1980 • 21 citations

Pure partial trisomy of the short arm of chromosome 5

1989 • 20 citations

Interstitial deletion, del(4)(q33q35.1), in a mother and two children.

1989 • 19 citations

The child with congenital anomalies and interstitial deletion of the long arm of chromosome 4

1982 • 19 citations

Second case report of del(4) (q25q27) and review of the literature

1991 • 18 citations

Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities.

1990 • 18 citations

Interstitial deletion of chromosome 4q diagnosed prenatally.

1986 • 15 citations

A new interstitial deletion of chromosome No. 4 del(4) (q22::q25)

1987 • 15 citations

Interstitial deletion of 4(q21q25) in a liveborn male

1991 • 15 citations

Toward the complete genomic map and molecular pathology of human chromosome 4

1994 • 14 citations

Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.

1982 • 12 citations

A new interstitial deletion of 4q (q21.1::q22.1).

1989 • 12 citations

Interstitial deletion of the long arm of chromosome 4, del(4)(q28→q31.3)

1995 • 11 citations

Prenatal diagnosis of and midtrimester pathology with karyotype 46,XY,del(4)(q22q26). A case report.

1990 • 8 citations

Newborn infant with del(9)(pter→q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary ears

1987 • 6 citations

Assignment of the aspartylglucosaminidase gene (AGA) to 4q33→q35 based on decreased activity in a girl with a 46, XX, del(4)(q33) karyotype

1992 • 5 citations

De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2–4q31.1

1991 • 3 citations