Khung‐Savatovsky, Suonavy
20  Ergebnisse:
Personensuche X
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3

Duplicated distal phalanx of thumb or hallux in trisomy 13:..:

Létard, Pascaline ; Guimiot, Fabien ; Dupont, Céline...
American Journal of Medical Genetics Part A.  176 (2018)  11 - p. 2325-2330 , 2018
 
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4

Inversion duplication deletions involving the long arm of c..:

Quelin, Chloe ; Spaggiari, Emmanuel ; Khung‐Savatovsky, Suonavy...
American Journal of Medical Genetics Part A.  164 (2014)  10 - p. 2504-2509 , 2014
 
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5

Pre‐ and postnatal phenotype of 6p25 deletions involving th..:

Delahaye, Andrée ; Khung‐Savatovsky, Suonavy ; Aboura, Azzedine...
American Journal of Medical Genetics Part A.  158A (2012)  10 - p. 2430-2438 , 2012
 
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6

Abnormal muscle development of the diaphragm in a fetus wit..:

Guilherme, Romain ; Guimiot, Fabien ; Tabet, Anne‐Claude...
American Journal of Medical Genetics Part A.  149A (2009)  12 - p. 2892-2897 , 2009
 
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8

Growth Restriction, Osteopenia, Placental Massive Perivillo..:

Abdulghani, Sahar ; Moretti, Felipe ; Nikkels, Peter GJ...
Pediatric and Developmental Pathology.  21 (2017)  1 - p. 91-94 , 2017
 
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10

Cytomegalovirus-Induced Brain Malformations in Fetuses:

Teissier, Natacha ; Fallet-Bianco, Catherine ; Delezoide, Anne-Lise...
Journal of Neuropathology & Experimental Neurology.  73 (2014)  2 - p. 143-158 , 2014
 
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12

Fetopathologic examination for early termination of pregnan..:

Gitz, Laurence ; Khung-Savatovsky, Suonavy ; Viot, Géraldine...
American Journal of Obstetrics and Gynecology.  205 (2011)  5 - p. 467.e1-467.e9 , 2011
 
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14

Expanding the genotypic and phenotypic spectrum of severe s..:

Abdelfattah, Fatima ; Kariminejad, Ariana ; Kahlert, Anne‐Karin...
Abdelfattah , F , Kariminejad , A , Kahlert , AK , Morrison , P J , Gumus , E , Mathews , K D , Darbro , B W , Amor , D J , Walsh , M , Sznajer , Y , Weiß , L , Weidensee , S , Chitayat , D , Shannon , P , Bermejo‐Sánchez , E , Riaño‐Galán , I , Hayes , I , Poke , G , Rooryck , C , Pennamen , P , Khung‐Savatovsky , S , Toutain , A , Vuillaume , ML , Ghaderi‐Sohi , S , Kariminejad , M H , Weinert , S , Sticht , H , Zenker , M & Schanze , D 2020 , ' Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders ' , Human Mutation , vol. 41 , no. 9 , pp. 1615-1628 . https://doi.org/10.1002/humu.24067.  , 2020
 
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