J. German

J. German, M. Reyes-Múgica, J. McNamara, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.

J. Kozloski, N. Ellis, J. German, 1994, American journal of human genetics.

Pseudovaginal perineoscrotal hypospadias

J. Opitz, J. Simpson, J. German, 1972, Clinical genetics.

III. DNA SYNTHESIS IN HUMAN CHROMOSOMES

J. German, 1962 .

Letter: Mongolism by tertiary trisomy.

J. German, R. Chaganti, G. Morillo-Cucci, 1975, Lancet.

Macrophage Apoptosis by Anthrax Lethal Factor Through p 38 MAP Kinase Inhibition

G. Boivin, A. Capobianco, K. Goss, 2002 .

The Bloom's syndrome gene product is homologous to RecQ helicases

N. Ellis, J. Groden, J. German, 1995, Cell.

Constitutional hyperrecombinability and its consequences.

J. German, 2004, Genetics.

Sclerosing hyaline necrosis of the liver in Bloom syndrome.

S. French, J. German, M. Cornford, 2009, Archives of pathology & laboratory medicine.

The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry.

N. Ellis, J. Groden, J. German, 1998, American journal of human genetics.

A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene

N. Ellis, J. Groden, J. German, 1998, Human mutation.

Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp

P. Goodfellow, N. Ellis, J. German, 1994, Nature Genetics.

Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization.

R. Chaganti, V. Murty, J. German, 1993, Cytogenetics and cell genetics.

Altered DNA ligase I activity in Bloom's syndrome cells

F. Becker, J. German, J. Chan, 1987, Nature.

Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients.

H. Takebe, J. German, N. Nakamura, 1989, Mutation research.

Xeroderma pigmentosum patients from Egypt: II. Preliminary correlations of epidemiology, clinical symptoms and molecular biology.

J. Cleaver, J. German, N. Hashem, 1981, The Journal of investigative dermatology.

Chromosome studies in “preleukemia”. III. myelofibrosis

P. Nowell, J. German, R. Chaganti, 1976, Cancer.

Molecular evidence that homologous recombination occurs in proliferating human somatic cells.

Y. Nakamura, J. Groden, J. German, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Bloom's syndrome. XIV. The disorder in Japan

H. Takebe, J. German, Hiraku Takebe, 1989, Clinical genetics.

Chromosomal breakage in human spermatozoa, a heterozygous effect of the Bloom syndrome mutation.

A. Rademaker, J. German, R. Martin, 1994, American journal of human genetics.

Abnormalities of human sex chromosomes

J. Simpson, J. German, M. Horwith, 1974, Humangenetik.

Studying human chromosomes today.

J. German, 1970, American scientist.

Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1.

P. Goodfellow, N. Ellis, J. Groden, 1996, Genomics.

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.

Z. Laron, E. Passarge, J. German, 1977, American journal of human genetics.

The Roberts syndrome

J. German, S. Temtamy, R. Schimke, 1974, Clinical genetics.

Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA.

R. Setlow, W. Carrier, J. German, 1969, Proceedings of the National Academy of Sciences of the United States of America.

MONGOLISM BY TERTIARY TRISOMY

J. German, R. Chaganti, G. Morillo-Cucci, 1975, The Lancet.

Bloom's Syndrome. XII. Report from the Registry for 1987

E. Passarge, J. German, 1989, Clinical genetics.

Bloom's syndrome. V. Surveillance for cancer in affected families

E. Passarge, J. German, D. Bloom, 1977, Clinical genetics.

Bloom's Syndrome. VII. Progress report for 1978

E. Passarge, J. German, D. Bloom, 1979, Clinical genetics.

Evidence for chromosome instability in vivo in bloom syndrome: Increased numbers of micronuclei in exfoliated cells

J. German, M. Rosin, 2004, Human Genetics.

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.

J. German, S. Schonberg, R. Chaganti, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Bloom's Syndrome Registry

E. Passarge, J. German, 1990, International journal of dermatology.

Sister chromatid exchange in cells metabolically coupled to Bloom's syndrome cells

J. German, S. Schonberg, 1980, Nature.

Mapping Human Autosomes: Assignment of the MN Locus to a Specific Segment in the Long Arm of Chromosome No. 2

J. German, R. Chaganti, 1973, Science.

THE cis AB PHENOTYPE IN THREE GENERATIONS OF ONE FAMILY: SEROLOGICAL, ENZYMATIC AND CYTOGENETIC STUDIES

J. German, W. Watkins, A. D. Yates, 1978, Journal of immunogenetics.

A retarded rate of DNA chain growth in Bloom's syndrome.

J. German, R. Hand, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes.

J. German, S. Schonberg, R. Chaganti, 1977, American journal of human genetics.

Bloom's syndrome and Fanconi's anemia: Demonstration of two distinctive patterns of chromosome disruption and rearrangement

J. German, T. Schroeder, 1974, Humangenetik.

Abnormalities of human sex chromosomes. V. A unifying concept in relation to the gonadal dysgeneses

J. German, 1970 .

Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest.

J. German, R. Chaganti, 1979, American journal of human genetics.

Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam.

J. Simpson, J. German, G. Mclemore, 1973, Annales de genetique.

Abnormal Y chromosomes and monosomy 45,X: a concept derived from the study of three patients.

J. German, G. Morillo-Cucci, 1971, Birth defects original article series.

Genetically determined sex-reversal in 46,XY humans

I. Merkatz, J. Simpson, J. German, 1978 .

Autoradiographic studies of human chromosomes

J. German, Dianne Aronian, 1969, Chromosoma.

Mapping Human Autosomes: Evidence Supporting Assignment of Rhesus to the Short Arm of Chromosome No. 1

F. Gardner, J. German, W. Marsh, 1974, Science.

In vitro labelling of human meiotic chromosomes with H3-thymidine.

A. Lima-de-faria, J. German, M. Ghatnekar, 2009, Hereditas.

Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth.

J. German, A. Sawitsky, D. Bloom, 1966, Annals of internal medicine.

Cytological Evidence for Crossing-Over in vitro in Human Lymphoid Cells

J. German, 1964, Science.

Gonadal dimorphism explained as a dosage effect of a locus on the sex chromosomes, the gonad-differentiation locus (GDL).

J. German, 1988, American journal of human genetics.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.

J. Lejeune, J. German, J. de Grouchy, 1964, Cytogenetics.

THE PATTERN OF DNA SYNTHESIS IN THE CHROMOSOMES OF HUMAN BLOOD CELLS

J. German, 1964, The Journal of cell biology.

Bloom's syndrome and EM9 cells in BrdU-containing medium exhibit similarly elevated frequencies of sister chromatid exchange but dissimilar amounts of cellular proliferation and chromosome disruption

J. German, J. H. Ray, 2004, Chromosoma.

Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum.

A. Adams, H. Evans, J. German, 1978, Cytogenetics and cell genetics.

Familial urinary tract anomalies.

J. Simpson, J. German, 1970, JAMA.

De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.

J. German, L. Friis, R. Chaganti, 1976, Annales de genetique.

Testicular feminisation and inguinal hernia.

J. Simpson, E. Passarge, J. German, 1973, Lancet.

Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p.

J. Simpson, J. German, F. Allen, 1971, Annales de genetique.

Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis.

J. Simpson, J. German, F. Allen, 1971, Annales de genetique.

AUTORADIOGRAPHIC STUDIES OF HUMAN CHROMOSOMES. I. A REVIEW.

J. German, 1969 .

Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development

H. Arnold, M. Wegner, G. Camerino, 2015, Journal of Medical Genetics.

Bloom's syndrome

R. Holliday, A. Spanos, J. German, 1986, Human Genetics.

XIII. DNA-polymerase activity of cultured lymphoblastoid cells

R. Holliday, A. Spanos, J. German, 1986 .

Bloom Syndrome: A Mendelian Prototype of Somatic Mutational Disease

J. German, 1993, Medicine.

Ulcerative colitis complicated by dysplasia-adenoma-carcinoma in a man with Bloom's syndrome.

S. French, J. German, J. Wang, 1999, Journal of clinical gastroenterology.

Cytogenetic evidence of the intrauterine origin of acute leukemia in monozygotic twins.

R. Chaganti, J. German, P. Meyers, 1979, The New England journal of medicine.

Bloom's syndrome protein, BLM, colocalizes with replication protein A in meiotic prophase nuclei of mammalian spermatocytes.

D. Walpita, J. German, T. Ashley, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal.

N. Ellis, J. German, T. Ye, 1999, American journal of human genetics.

Bloom's syndrome: DNA replication in cultured fibroblasts and lymphocytes

J. German, R. Hand, 1977, Human Genetics.

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

M. Leppert, N. Ellis, J. German, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Bloom's syndrome cells have an abnormal serum growth response.

J. Lechner, J. Groden, A. Jetten, 1983, Experimental cell research.

Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder

J. German, D. Bloom, L. Crippa, 2004, Chromosoma.

Roberts' syndrome.I. Cytological evidence for a disturbance in chromatid pairing

J. German, 1979, Clinical genetics.

Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation

G. Boivin, A. Capobianco, K. Goss, 2002, Science.

Long‐term study of the immunodeficiency of Bloom's syndrome

J. German, T. Orii, N. Kuwabara, 1992, Acta paediatrica.

Polymorphic chromosomes and gene assignment in man.

J. German, R. Chaganti, L. Weitkamp, 1975, Birth defects original article series.

BLM, the Bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins

N. Ellis, W. Holloman, J. German, 2001, Cytogenetic and Genome Research.

Abnormal immune responses of Bloom's syndrome lymphocytes in vitro.

J. German, S. D. Litwin, T. Hütteroth, 1975, The Journal of clinical investigation.

Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome.

W. Bigbee, R. Jensen, J. German, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Syndrome‐causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry

N. Ellis, J. German, T. Ye, 2007, Human mutation.

Human chromosomal deletion: two patients with the 4p- syndrome.

M. A. Engle, E. Passarge, J. German, 1970, The Journal of pediatrics.

PBDX is the XG blood group gene

P. Goodfellow, N. Ellis, G. Banting, 1994, Nature Genetics.

Bloom's syndrome

J. German, D. Bloom, 1972, Humangenetik.

Developmental anomaly resembling the trisomy 18 syndrome.

J. Simpson, J. German, 1969, Annales de genetique.

A test for Fanconi's anemia.

J. German, D. Warburton, S. Schonberg, 1987, Blood.

Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.

C. Eng, R. Desnick, N. Ellis, 1998, Molecular genetics and metabolism.

An abnormal profile of DNA replication intermediates in Bloom's syndrome.

J. German, U. Lönn, U. Nylén, 1990, Cancer research.

Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity

N. Ellis, J. German, M. Proytcheva, 1996, Clinical genetics.

Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locus.

J. Groden, J. German, 1992, Human genetics.

Impaired immune function in patients with xeroderma pigmentosum.

C. Bucana, M. Kripke, J. Cleaver, 1985, Cancer research.

A previously unrecognized X-linked syndrome of dysmorphia.

J. Simpson, J. German, J L Simpson, 1975, Birth defects original article series.

Different mutations are responsible for the elevated sister-chromatid exchange frequencies characteristic of Bloom's syndrome and hamster EM9 cells.

J. German, E. Louie, J. H. Ray, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Autoradiographic studies of human chromosomes

E. Passarge, J. German, J. Rock, 2004, Chromosoma.

[Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].

I. Emerit, C. Sureau, J. German, 1970, Annales de Genetique.

Analysis of a BrdU-sensitive site in the cactus mouse (Peromyscus eremicus): chromosomal breakage and sister-chromatid exchange

N. Schneider, J. German, R. Chaganti, 2004, Chromosoma.

IDENTIFICATION AND CHARACTERIZATION OF HUMAN CHROMOSOMES BY DNA REPLICATION SEQUENCE

J. German, 1964 .

Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.

J. Simpson, J. German, M. Horwith, 1974, Humangenetik.

Human chromosomal deletion: with the 4p-syndrome Two patients

E. Passarge, J. German, A. Engle, 1970 .

The linkage relationships of marker sites on chromosomes no. 2 and 10

J. German, R. Chaganti, L. Weitkamp, 1978, Annals of human genetics.

Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditism.

J. Simpson, J. German, G. Morillo-Cucci, 1971, Birth defects original article series.

Analysis of Sister‐Chromatid Exchanges

J. German, Becky Alhadeff, Becky Alhadeff, 1994, Current protocols in human genetics.

Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. 1969.

R. Setlow, W. Carrier, J. German, 2004, DNA repair.

Increased amounts of hybrid (heavy/heavy) DNA in Bloom's syndrome fibroblasts.

R. Waters, J. German, J. Regan, 1978, Biochemical and biophysical research communications.

Sensitivity of Bloom's syndrome lymphocytes to ethyl methanesulfonate

J. Heddle, J. German, A. Krepinsky, 2004, Human Genetics.

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

C. Falk, J. Simpson, J. German, 1974, Humangenetik.

A marrow chromosomal abnormality preceding clinical leukemia in Down's syndrome.

J. German, M. Erlandson, A. Demayo, 1967, Blood.

Chronic renal disease, myotonic dystrophy, and gonadoblastoma in XY gonadal dysgenesis

J. Simpson, J. German, J. Mouradian, 1982, Journal of Medical Genetics.

The chromosome-breakage syndromes: rare disorders that provide models for studying somatic mutation.

J. German, 1990, Birth defects original article series.

Genetically Determined Sex‐Reversal in 46, XY Humans

I. Merkatz, J. Simpson, J. German, 1979, Science.

Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations.

D. Bootsma, J. German, M. Niermeijer, 1984, American journal of human genetics.

Autoradiographic studies of human chromosomes. II. Data concerning the position of the MN locus.

J. German, F. Allen, M. Walker, 1969, Vox Sanguinis.

Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs.

J. Simpson, J. German, M. New, 1971, Birth defects original article series.

Males with a uterus and fallopian tubes, a rare disorder of sexual development.

J. German, G. Morillo-Cucci, 1971, Birth defects original article series.

The syndrome of congenital telangiectatic erythema and stunted growth.

J. German, D. Bloom, 1971, Archives of dermatology.

Bloom's syndrome XI. Progress report for 1983

E. Passarge, J. German, D. Bloom, 1984, Clinical genetics.

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

N. Ellis, J. German, M. Leppert, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Cytogenetic Investigation of the Rhnull Phenotype 1

J. German, W. Marsh, R. Chaganti, 1974 .

DNA REPAIR DEFECTS AND HUMAN DISEASE

J. German, 1978 .

Autoradiographic studies of human chromosomes

J. German, L. Crippa, Melvin S. Schwartz, 2004, Chromosoma.