P. Bowen

发表

Inverted duplication of 22pter----q11.21 in cat-eye syndrome.

C. Lin, J. Hoo, A. Robertson, 1986, American journal of medical genetics.

Workshop on genetic disorders in the Hutterites--Edmonton, Canada, October 12-13, 1983.

P. Bowen, 1985, American journal of medical genetics.

Trembling chin — a report of this inheritable dominant character in a four‐generation Canadian family

J. Bamforth, P. Bowen, D. Alsager, 1991, Clinical genetics.

Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites.

P. Bowen, V. Schurig, A. Orman, 1981, American journal of medical genetics.

Spontaneous abortion. Chromosome studies on 41 cases and an analysis of maternal age and duration of pregnancy in relation to karyotype.

P. Bowen, C. S. Lee, 1969, American journal of obstetrics and gynecology.

Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities

C. Lin, J. Hoo, P. Bowen, 1987, Human Genetics.

Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).

R. Gardner, P. H. Fitzgerald, P. Bowen, 1983, American journal of medical genetics.

International Standing Committee on Human Cytogenetic Nomenclature

Y. Rumpler, Uta Francke, Elaine H. Zackai, 1976 .

Ectodermal dysplasia, mental retardation, cleft lip/palate and other anomalies in three sibs

P. Bowen, H. Armstrong, 1976, Clinical genetics.

Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.

T. Unger, J. Meyne, C. Lin, 1990, American journal of medical genetics.

HEREDITARY MALE PSEUDOHERMAPHRODITISM WITH HYPOGONADISM, HYPOSPADIAS, AND GYNECOMASTIA: REIFENSTEIN'S SYNDROME.

V. McKusick, C. Migeon, C J MIGEON, 1965, Annals of internal medicine.

Chromosomes of the Walker 256 rat mammary carcinoma: observations on primary and metastatic tumors of a new subline with a pseudodiploid karyotype.

P. Bowen, O. Thurston, S. Nicholson, 1968, Journal of the National Cancer Institute.

Partial trisomy 4q due to familial 2/4 translocation

P. Bowen, B. Biederman, 1976, Human Genetics.

Partial trisomy 12p due to t(12;21)pat translocation

D. Schiff, P. Bowen, B. Biederman, 2004, Human Genetics.

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS.

P. Bowen, H. Zellweger, R. Lindenberg, 1964, Bulletin of the Johns Hopkins Hospital.

Caudal regression anomalad (sacral agenesis) in siblings

N. Finer, P. Bowen, L. Dunbar, 1978, Clinical genetics.

Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement

H. Pabst, R. Collins-Nakai, J. Hoo, 1986, Clinical genetics.

Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements.

K. Ying, P. Bowen, C. S. Lee, 1974, American journal of human genetics.

Interchromosomal duplication for the short arm of chromosome no. 9: report of three cases due to a familial translocation t(9; 11) and one case with a de novo 47, XX, +9p karyotype.

C. Lin, P. Bowen, B. Biederman, 2008, Journal of mental deficiency research.

Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect.

P. Bowen, B. Biederman, 1976, Annales de genetique.

FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS.

P. Bowen, H. Rosenblum, L. Linsao, 1964, The New England journal of medicine.

The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.

J. Hoo, P. Bowen, B. Biederman, 1985, Annales de genetique.

Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7

P. Bowen, B. Biederman, 1978, Human Genetics.

Balanced Reciprocal Translocation Between Two D‐Group Chromosomes in a Family with Myotonic Dystrophy

P. Bowen, J. C. Harvey, C. S. Lee, 1968, The American journal of the medical sciences.

The Laurence-Moon syndrome. Association with hypogonadotrophic hypogonadism and sex-chromosome aneuploidy.

M. Ferguson-Smith, H. G. Butler, P. Bowen, 1965, Archives of internal medicine.

Serum protein polymorphisms in Indians of western Canada. Gene frequencies and data on the Gc-albumin linkage.

P. Bowen, F. O'Callaghan, C. S. Lee, 1971, Human heredity.

Polydactyly and other minor stigmata associated with 46,XX-47,XX,D+ mosaicism.

P. Bowen, C. S. Lee, H. Armstrong, 1970, Canadian Medical Association journal.

Comparison of Non‐Modal Chromosome Counts in Individuals Affected with Myotonic Dystrophy and in Control Subjects

J. Mcgregor, P. Bowen, J. C. Harvey, 1968, American Journal of the Medical Sciences.

The X-linked syndrome of macroorchidism and mental retardation: further observations.

P. Bowen, K. Swallow, B. Biederman, 1978, American journal of medical genetics.

A (2;4) translocation, balanced, 46 chromosomes. Repository identification No. GM-1064.

P. Bowen, A. Greene, L. Coriell, 1976, Cytogenetics and Cell Genetics.

5 Chromosomal Abnormalities

P. Bowen, 1964 .

A genetic linkage analysis of chromosome 6 markers Chido, HLA, and glyoxalase.

A. Steinberg, E. Giblett, D. Singal, 1976, Cytogenetics and Cell Genetics.

PH-1 CHROMOSOME IN THE DIAGNOSIS OF CHRONIC MYELOID LEUKEMIA: REPORT OF A CASE WITH FEATURES SIMULATING MYELOFIBROSIS.

P. Bowen, C. S. Lee, 1963, Bulletin of the Johns Hopkins Hospital.