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1

Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries

Maurizio Clementi, Romano Tenconi, Fabrizio Bianchi, Claude Stoll

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 61 KB

english, 2000

2

Omphalocele and gastroschisis and associated malformations

Claude Stoll, Yves Alembik, Beatrice Dott, Marie-Paule Roth

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 64 KB

english, 2008

3

On the symmetry of limb deficiencies among childrenwith multiple congenital anomalies

Claude Stoll, Aldo Rosano, Lorenzo D Botto, David Erickson, Muin J Khoury, Richard S Olney, Eduardo E Castilla, Guido Cocchi, Martina C Cornel, Janine Goujard, Eva Bermejo, Paul Merlob, Osvaldo Mutchi

Journal:

Annales de Génétique

Year:

2001

Language:

english

File:

PDF, 39 KB

english, 2001

4

La, Ce, Nd, and Sr behavior in minette magmas during crystallization of apatite-clinopyroxene-mica paragenesis at upper-mantle conditions

Plá Cid, Jorge, Nardi, Lauro V. Stoll, Campos, Cristiani S., Gisbert, Pere Enrique, Merlet, Claude, Conceiçao, Herbet, Boyer, Bernard

Journal:

European Journal of Mineralogy

Year:

2007

Language:

english

File:

PDF, 841 KB

english, 2007

5

Different Policies on Prenatal Ultrasound Screening Programmes and Induced Abortions Explain Regional Variations in Infant Mortality with Congenital Malformations

Garne, Ester, Berghold, Andrea, Johnson, Zachary, Stoll, Claude

Journal:

Fetal Diagnosis and Therapy

Year:

2001

Language:

english

File:

PDF, 160 KB

english, 2001

6

Associated anomalies in cases with anorectal anomalies

Stoll, Claude, Dott, Beatrice, Alembik, Yves, Roth, Marie‐Paule

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 1.70 MB

english, 2018

7

Associated anomalies in cases with congenital clubfoot

Stoll, Claude, Alembick, Yves, Dott, Beatrice, Roth, MarieâPaule

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 1.19 MB

2020

8

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: Report of three patients

Fokstuen, Siv, Bottani, Armand, Medeiros, Paula F. V., Antonarakis, Stylianos E., Stoll, Claude, Schinzel, Albert

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 394 KB

english, 1997

9

Classification of limb defects

Stoll, Claude, Duboule, Denis, Holmes, Lewis B., Spranger, J�rgen

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 27 KB

english, 1998

10

Limb defects associated with major congenital anomalies: Clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems

Aldo Rosano, Lorenzo D. Botto, Richard S. Olney, Muin J. Khoury, Annukka Ritvanen, Janine Goujard, Claude Stoll, Guido Cocchi, Paul Merlob, Osvaldo Mutchinick, Martina C. Cornel, Eduardo E. Castilla,

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 112 KB

english, 2000

11

Problems in the diagnosis of fragile X syndrome in young children are still present

Pr. Claude Stoll

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 215 KB

english, 2001

12

Osteomesopyknosis: An autosomal dominant osteosclerosis

Dr. Claude G. Stoll, Dominique Collin, Jean Dreyfus, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1981

Language:

english

File:

PDF, 262 KB

english, 1981

13

Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome

Dr. Claude Stoll, André Geraudel, Henri Berland, Marie-Paule Roth, Béatrice Dott, Lewis B. Holmes, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1985

Language:

english

File:

PDF, 274 KB

english, 1985

14

A supraumbilical midline raphé with sternal cleft in a 47,XXX woman

Claude Stoll, Myriam Vivier, Robert Renaud, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 345 KB

english, 1987

15

Dandy-walker variant malformation, spastic paraplegia, and mental retardation in two sibs

Claude Stoll, Christian Huber, Yves Alembik, Eliette Terrade, Daniel Maitrot

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 458 KB

english, 1990

16

Epidemiology of Down syndrome in 118,265 consecutive births

Dr. Claude Stoll, Yves Alembik, Béatrice Dott, Marie-Paule Roth

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 596 KB

english, 1990

17

New X-linked syndrome of mental retardation, short stature, and hypertelorism

Prof. Claude Stoll, André Géraudel, Annick Chauvin

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 465 KB

english, 1991

18

Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin sequence in three generations: A new inherited MCA syndrome?

Professor Claude Stoll, Jean-René Kieny, Béatrice Dott, Yves Alembik, Sonya Finck

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 568 KB

english, 1992

19

Parental consanguinity as a cause of increased incidence of birth defects in a study of 131, 760 consecutive birthsxs

Professor Claude Stoll, Yves Alembik, Béatrice Dott, Josué Feingold

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 401 KB

english, 1994

20

Reply to Doctor Bottani on our family with X-linked mental retardation, short stature, and hypertelorism

Dr., Professor Claude Stoll

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 58 KB

english, 1994

21

Reply to Newton Freire-Maia on inbreeding among medical geneticists II

Professor Claude Stoll, Yves Alembik, Béatrice Dott, Josué Feingold

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 68 KB

english, 1995

22

Polysyndactyly, complex heart malformations cardiopathy, and hepatic ductal plate anomalies: An autosomal recessive syndrome diagnosed antenatally

Claude Stoll, B. Gasser

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 192 KB

english, 2003

23

Associated malformations in patients with oral clefts

Claude Stoll, Yves Alembik, Beatrice Dott, Marie-Paule Roth

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 68 KB

english, 2007

24

Associated malformations among infants with neural tube defects

Claude Stoll, Beatrice Dott, Yves Alembik, Marie-Paule Roth

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 90 KB

english, 2011

25

Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

Ester Garne, Maria Loane, Catherine de Vigan, Gioacchino Scarano, Hermien de Walle, Yves Gillerot, Claude Stoll, Marie-Claude Addor, David Stone, Blanca Gener, Maria Feijoo, Carmen Mosquera-Tenreiro,

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 104 KB

english, 2004

26

Prenatal diagnosis of congenital my asthenia with arthrogryposis in a myasthenic mother

Claude Stoll, Marie-Christine Ehret-Mentre, Alain Treisser, Christine Tranchant

Journal:

Prenatal Diagnosis

Year:

1991

Language:

english

File:

PDF, 493 KB

english, 1991

27

Evaluation of prenatal diagnosis by a registry of congenital anomalies

Claude Stoll, Yves Alembik, Béatrice Dott, Marie-Paule Roth, Sonja Finck

Journal:

Prenatal Diagnosis

Year:

1992

Language:

english

File:

PDF, 446 KB

english, 1992

28

Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registries

Martin C. H. Haeusler, Andrea Berghold, Claude Stoll, Ingeborg Barisic, Maurizio Clementi

Journal:

Prenatal Diagnosis

Year:

2002

Language:

english

File:

PDF, 83 KB

english, 2002

29

Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population

Claude Stoll, Béatrice Dott, Yves Alembik, Marie-Paule Roth

Journal:

Year:

1993

Language:

english

File:

PDF, 474 KB

english, 1993

30

Cytogenetic findings in 122 couples with recurrent abortions

Journal:

Year:

1981

Language:

english

File:

PDF, 212 KB

english, 1981

31

4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat

Claude Stoll, A. Pennerath, Ch. Lausecker

Journal:

Year:

1981

Language:

english

File:

PDF, 208 KB

english, 1981

32

Balanced familial translocation t(5;19) (q12;p or q11) with phenotypical abnormalities in a girl

Claude Stoll, Jean-Marc Levy, Maxime Champy

Journal:

Year:

1975

Language:

english

File:

PDF, 1.19 MB

english, 1975

33

Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13)

Claude Stoll, Jean-Marc Levy, Alexandre Gardea

Journal:

Year:

1975

Language:

english

File:

PDF, 1.08 MB

english, 1975

34

Nonrandom distribution of exchange points in patients with reciprocal translocations

Journal:

Year:

1980

Language:

english

File:

PDF, 377 KB

english, 1980

35

A case of Down's syndrome resulting from mirror duplication of chromosome 21

Claude Stoll, A. Pennerath, Ch. Lausecker

Journal:

European Journal of Pediatrics

Year:

1982

Language:

english

File:

PDF, 494 KB

english, 1982

36

SIMS analyses on trace and rare earth elements in coexisting clinopyroxene and mica from minette mafic enclaves in potassic syenites crystallized under high pressures

Jorge Plá Cid, Lauro Valentim Stoll Nardi, Pere Enrique Gisbert, Claude Merlet, Bernard Boyer

Journal:

Contributions to Mineralogy and Petrology

Year:

2005

Language:

english

File:

PDF, 645 KB

english, 2005

37

SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations

Philippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, Victor Chan, Serge Perelman, Tanya Stojkovic, Claude Stoll, Christophe Vial, François Ziegler, Antoon Vandenberghe, Irène Maire

Journal:

Journal of the Peripheral Nervous System

Year:

2006

Language:

english

File:

PDF, 783 KB

english, 2006

38

A gene for achondroplasia–hypochondroplasia maps to chromosome 4p

Merrer, Martine Le, Rousseau, Francis, Legeai-Mallet, Laurence, Landais, Jean-Christophe, Pelet, Anna, Bonaventure, Jacky, Sanak, Marek, Weissenbach, Jean, Stoll, Claude, Munnich, Arnold

Journal:

Nature Genetics

Year:

1994

File:

PDF, 404 KB

1994

39

Genetic Epidemiology

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 41 KB

english, 2005

40

Clinical genetics: Medical genetics

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 36 KB

english, 2006

41

Role of Glial Cell Line-Derived Neurotrophic Factor in Germ-Line Stem Cell Fate

LAURA BRAYDICH-STOLLE, COURTNEY NOLAN, MARTIN DYM, MARIE-CLAUDE HOFMANN

Journal:

Annals of the New York Academy of Sciences

Year:

2005

Language:

english

File:

PDF, 311 KB

english, 2005

42

Immortalization of Mouse Germ Line Stem Cells

Marie-Claude Hofmann, Laura Braydich-Stolle, Luis Dettin, Eric Johnson, Martyn Dym

Journal:

Year:

2005

Language:

english

File:

PDF, 388 KB

english, 2005

43

Associated malformations among infants with anophthalmia and microphthalmia

Claude Stoll, Beatrice Dott, Yves Alembik, Marie-Paule Roth

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2012

Language:

english

File:

PDF, 727 KB

english, 2012

44

Non-random clonal evolution in 45 cases of chronic myeloid leukemia

Claude Stoll, Francis Oberling

Journal:

Leukemia Research

Year:

1979

Language:

english

File:

PDF, 348 KB

english, 1979

45

Evolution: Mark Ridley; Blackwell Science, 2004, 751 pp., 3rd Edition

Journal:

Annales de Génétique

Year:

2004

Language:

english

File:

PDF, 69 KB

english, 2004

46

Principles of Human Evolution: Roger Lewin, Robert Foley; Blackwell Publishing Blackwell Science, 2004, 576 pp., 2nd Edition

Journal:

Annales de Génétique

Year:

2004

Language:

english

File:

PDF, 23 KB

english, 2004

47

Genomics Applications in Human Biology

Journal:

Annales de Génétique

Year:

2004

Language:

english

File:

PDF, 89 KB

english, 2004

48

Progressive osseous heteroplasia: an uncommon cause of ossification of soft tissues

Claude Stoll, Marie-Rose Javier, Jean-Pierre Bellocq

Journal:

Annales de Génétique

Year:

2000

Language:

english

File:

PDF, 564 KB

english, 2000

49

Prenatal sonographic diagnosis of skeletal dysplasias. A report of 47 cases

Bérénice Doray, Romain Favre, Brigitte Viville, Bruno Langer, Michel Dreyfus, Claude Stoll

Journal:

Annales de Génétique

Year:

2000

Language:

english

File:

PDF, 80 KB

english, 2000

50

Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination

Claude Stoll, Béatrice Dott, Yves Alembik, Marie-Paule Roth

Journal:

Annales de Génétique

Year:

2000

Language:

english

File:

PDF, 44 KB

english, 2000